ZMP
si:ch211-245p7.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate hydrocephalus inducing (HYDIN) [Source:UniProtKB/TrEMBL;Acc:Q1LW
Human Orthologues:
AC109135.1, AL360154.1, HYDIN
Human Description:
hydrocephalus inducing homolog (mouse) [Source:HGNC Symbol;Acc:19368]
Mouse Orthologue:
Hydin
Mouse Description:
hydrocephalus inducing Gene [Source:MGI Symbol;Acc:MGI:2389007]
Alleles
There are 28 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32204 | Nonsense | Available for shipment | Available now |
sa43099 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43100 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17962 | Nonsense | Available for shipment | Available now |
sa10786 | Essential Splice Site | Available for shipment | Available now |
sa36644 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12926 | Nonsense | Available for shipment | Available now |
sa43101 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12486 | Essential Splice Site | Available for shipment | Available now |
sa39199 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43102 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36645 | Essential Splice Site | Available for shipment | Available now |
sa43103 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29030 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43104 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8483 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17202 | Nonsense | Available for shipment | Available now |
sa25063 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43105 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16299 | Splice Site, Nonsense | Available for shipment | Available now |
sa12927 | Nonsense | Available for shipment | Available now |
sa14679 | Nonsense | Available for shipment | Available now |
sa43106 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32205 | Nonsense | Available for shipment | Available now |
sa44889 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23295 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32204
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 72 | 4812 | 2 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | Nonsense | 72 | 1146 | 2 | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21057182)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21287405 |
GRCz11 | 18 | 21276471 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTAACCACAGAAGAGCGATTATCAAACACATTTGAGATGCGTCCGCCT[C/T]GAATCTTGGAGCTCTTAGACATGAGCGAAACCACACATCACAAGGTAAAA
Long Flanking Sequence:
ATTTGACCAGTTAGCCAAAGGGTAATCAAATCAGTCTTGCTTTTTTGATTCTGATTAGAGCAATCAATCTCTTTTTAGAGACTTTAAAAAAGTTTATGCCAGGCTTGAAGAAAAATAATTGAAAAATAATAACATTTTTTAAATGGTTGTCTATATATATCGCACATTTCATACACAGTGGTAATTCAAAGTGCTTTACATAAACGGAAATAAAACAGACAAGTATAAGAAAACAAAAACATATTATACATTCAATTTATTTTTTATTTTTTTAATCATTCTTTTACAATACATGTTTTGCCCAAACTTTTTTTTTCAAAGAATAATGCATGCAACATAAAATACTGCTGTAGAAAAAGCACAATATTTTTTTCATTGTATACATGTGCACTCAGAACAGCTTGAATATGTCTTTGCAGCTGATCCCATCTGTATATGCTCGAGAAATGAGCCTAACCACAGAAGAGCGATTATCAAACACATTTGAGATGCGTCCGCCT[C/T]GAATCTTGGAGCTCTTAGACATGAGCGAAACCACACATCACAAGGTAAAATGCCATTATTTTAGCATGCTCAGCTCCAGTGCTTAATTAATTAGTTTGCTCTTCTACATCACTGGCTGCATCCCTTAGCAGCAACATTTTCAAAGTCGATTAAGGTCATTATTATAGTTTCTCTCTGGGAGATACTGAAGGCTTTTAAAATGCGCAGTATAGCAATTGTAGCTGTTTATAGTACTTTTGAATGCCAGGTTTTTTATACTGACTCAATATTGACTAATACAAATGTAAGGCAAACTACAGAATGTCACCTTTGAATTTAAAAAGAAATAACAGAGCTATTATCATGACAGTGCTATGACCAGCCATATAAGTAAAGGGTTAACCATTTTTTTCCAGTAAAATTTATATTTTAATTATGCAAAAATATATTTAATGATCTTTTTTCATACTGAAGATAAAATATAGAAGCGATTTTAAATGTACATTTTTTTCAGATATCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43099
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 168 | 4812 | 4 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | Nonsense | 168 | 1146 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21060711)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21290934 |
GRCz11 | 18 | 21280000 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAAGTGGCTCCAGGCATGGCATCTACATTCACCATTCTCTTCACTCCA[C/T]AAGAGAACAAGGTAAATTTGTTAGTTCCAATAGAAATGCAATTGACGCTG
Long Flanking Sequence:
TTTCTAGACCATCTTGCAATATTCCTTTAAAACATTTGCAGATTATGTTGTCCATTTTCCTGTATAATGATCCATGACTTAATGTAGACTGACTAGTTGCTGACTACTGCAGATTCCTGAACTTGTAAAGGTTATCGAAGAAGACCATATGAACATATTTCCTATTAAAGCTAAAATAAGGAAGCCAATGCCATTTTACATTTTGTCAGATGTCTGCTAATATATATCACATTTGACTCTTATATATTTTTCCTATTTAAAATTTCATATTCATTGGTGACATGCACTATTTAACATATTGCTTTATTCCGTCAAGACAATTCATAATTCTATTCAATGTATATTCATCGCTGGCTTAATGTAACTAACTATTGCAGGTTCCTCGACTGGTAAAGGTGATTGTTGAAGACTCACTGTATTTTAAAGTGGTGAGCCCACTAGATGTTAGTAAGAAAGTGGCTCCAGGCATGGCATCTACATTCACCATTCTCTTCACTCCA[C/T]AAGAGAACAAGGTAAATTTGTTAGTTCCAATAGAAATGCAATTGACGCTGTTTTATTGGTTATACATCAAACTCTATTGCTGGTGCACCTCTGGGACATTTGCTTGTATTTTTAATGAATGACCAAGAAAATTTGAATTCAGTTCAATTCAATTCATGTTTATGTGGTGCTTTAACAATATAGATTGTGTCAAAGCAGCTTAACATATTGAAGTTCTAATAAATTGAAACTGTGTCAGTCCAGTGTTGTTTAATTTTTTCTGTTGAAAGTCCAAACACTGAAGAGCAAACCCATCGATGCGCAGCTCCACAAGTACCAAGTTAATATAAAACACTGTCTTGTAAATAAACTTTAACATCAAGTTAACATATAATTTCTGATAAACTGAGAAGAGCACAGGGCACTAGAGACTTAGGGCTCTATTTTGACGATCCATGCGCAAAGTCCAAAGCGCAGGGCGCAAACGCATTAAGGGCGTGTCAGAATCCACTTTTGCTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43100
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Essential Splice Site | 238 | 4812 | 5 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | Essential Splice Site | 238 | 1146 | 5 | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21063149)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21293372 |
GRCz11 | 18 | 21282438 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACGAAACATAGGAAATTGTGAGGCTAAATTCAAGCTTAGCACATGCAG[G/A]TAAGAGAGCAGCGTCAGTGCAAATTGCTTTGACATTGTAGTACGAAGACA
Long Flanking Sequence:
TCTAGGTGGTGCGGGAGCAGTGTAATCTTTTTTAGGGGGCTTATATTTTTGATAATTTTTCTCTTTTGTCCAAAAAGCGAACATGCATTTTTCAGGCAATATCTTTCTGAAAATTATGTGCATCCTGGTAAAGAGTTTTTTTTACCACTGAAATAATTATAGAGTCATTATTTAAAAGTTAAAAAAAATTTTTTTGTTGCTTTTAATAGTTAAATACTCAAAGAGTAAGACTAGTCTTAGTCTTGAAGCTACATACTGCCTCTCTTAACAGCCACTGACAATCCGATGCTTGAATCGCAGGATTATATCCACAGTGTCATCTGTGTGACTGAACGTGAGAAGTTTGAGGTGCCCATTCGTGCGATTGGACCCCGTGCCATCTTGGACTTTCCAGACAGTCTCCATTTCTTAGTGTGTCCAGTCAAGTGCTTATCCCAGAGAACTCTGCTTGTACGAAACATAGGAAATTGTGAGGCTAAATTCAAGCTTAGCACATGCAG[G/A]TAAGAGAGCAGCGTCAGTGCAAATTGCTTTGACATTGTAGTACGAAGACAGTGTGTCTGTAATGATGTATGTGTTCCCAACAGGCCGTTTTCTGTAGAGCCATCTGTAGGGACGCTTATTGCTGGTCAATGCATGCAAGTTACTGTTGGGTTCATGCCTAAAACCACAGGGGATCACAGTCAGGTTTTGCTGCTGCACTACCATTCAGGTACTTGCTGCTAATTACATCACCACAATCTGCTCTTCCCACAAACTCCTCTTCTGCACACGGCTATATGTCACTGTGACACAAATACTGATTTCCTCATCTCCAGCCCACTCACATGTGTAAATGATCTTATTATTAAGCTTCACGATTAATGTCTCATCACATTTTTTTATACTTTCATAATTACTAAAGTTTTCATGTATTAATGCTCTTTACTTCTCACAGCCTGCACAGACACAAATGTGGGTGACATTTGAAAGTAAAACATCACATTGACACATCACATAAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17962
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 1015 | 4812 | 20 | 81 |
ENSDART00000100830 | Nonsense | 29 | 140 | 2 | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21111712)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21341935 |
GRCz11 | 18 | 21331001 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTGAGTGTTTWATAAATTGCAGGTGGTTACAGAGAAGCTTGTATGCTA[T/A]GCTGTTATCGGGAGGCAATATGTGAGGGAGTGCATCATCACTGCAGACGT
Long Flanking Sequence:
GCTGCACTTAATCCTCTTTTAGTGGAGCAGCATGGAGCTGTGTATTGACTTCCTCTCACGAGCATTGCAGAGATGCATGCCTCCTTGAATCCTTATTGATTTAATGGTAAATCAGAGATGAGAGAAGGTGAGAAGTGAATATAGGCCTGACCTGCTGCATCCCACGCCGGGCTGCTGCATTGCTTAGCCATCAGTCGCCGGGATGTCAGTGCACCGACTCTCAGCCTTCATAGAGAAGTTCTCTGTTTTAGTGACAAAGCTGAGCAGGCTTTTGAAAGGTCAAACTATCAAAGATTATTCACATCTATTCATATATTGAGAATACGAAAATGATTTTGTATACGCTATTACCCGAGTTCTGCCAAAAAGTGTTGCACATTGATTTTTTGTGTGCTTTGTGTTAATTCTTTTCCCCCATTGCATTCATTTTAAAATGTTACATATCATTAAATGTGAGTGTTTTATAAATTGCAGGTGGTTACAGAGAAGCTTGTATGCTA[T/A]GCTGTTATCGGGAGGCAATATGTGAGGGAGTGCATCATCACTGCAGACGTCACATGTCAGTTTGTCTCCCCAGCAGTTGAGATCTCCTCCCAGCAACTCAACTTCTATGTAGAAAAGGTTTGCAAAAAAGAATTTTATGTTAATTTATTTACAAATTTATTTTAACAAAATGTTCTGGTTTCATTTTATTTATTTAGTTTCTGTGTTTCAGGACCGCCAAGTTTAATACACTAAACTTAAATACAAATTTAAGGACGGTCACATTTTATTGCAAGCAAGTTTTAAACTTTTATTAAATTAATTTATGACTCTTTTTTATTTTTCACCTTTTATTAGTTTATTTTTTTATTTATCTATATATTGTAGTTAAATTTTTGGTGACACTTAACAAGGTTTTGTTTGTTAACAGTAGTTAAATATCTGTCATGTCATGGTTACGGCAAGGTTAGAAAGGAATAACGGTTAGTAATGTTATGCTCTGTTCACACCAGAAGCCGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10786
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Essential Splice Site | 1054 | 4812 | 20 | 81 |
ENSDART00000100830 | Essential Splice Site | 68 | 140 | 2 | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21111830)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21342053 |
GRCz11 | 18 | 21331119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCCAGCAGTTGAGATCTCCTCCCAGCAACTYAACTTCTATGTAGAAAAG[G/A]TTTGCAAAAAAGAATTTTATGWTAATTTATTTACAAATTTATTTTAACAA
Long Flanking Sequence:
TGAGAGAAGGTGAGAAGTGAATATAGGCCTGACCTGCTGCATCCCACGCCGGGCTGCTGCATTGCTTAGCCATCAGTCGCCGGGATGTCAGTGCACCGACTCTCAGCCTTCATAGAGAAGTTCTCTGTTTTAGTGACAAAGCTGAGCAGGCTTTTGAAAGGTCAAACTATCAAAGATTATTCACATCTATTCATATATTGAGAATACGAAAATGATTTTGTATACGCTATTACCCGAGTTCTGCCAAAAAGTGTTGCACATTGATTTTTTGTGTGCTTTGTGTTAATTCTTTTCCCCCATTGCATTCATTTTAAAATGTTACATATCATTAAATGTGAGTGTTTTATAAATTGCAGGTGGTTACAGAGAAGCTTGTATGCTATGCTGTTATCGGGAGGCAATATGTGAGGGAGTGCATCATCACTGCAGACGTCACATGTCAGTTTGTCTCCCCAGCAGTTGAGATCTCCTCCCAGCAACTCAACTTCTATGTAGAAAAG[G/A]TTTGCAAAAAAGAATTTTATGTTAATTTATTTACAAATTTATTTTAACAAAATGTTCTGGTTTCATTTTATTTATTTAGTTTCTGTGTTTCAGGACCGCCAAGTTTAATACACTAAACTTAAATACAAATTTAAGGACGGTCACATTTTATTGCAAGCAAGTTTTAAACTTTTATTAAATTAATTTATGACTCTTTTTTATTTTTCACCTTTTATTAGTTTATTTTTTTATTTATCTATATATTGTAGTTAAATTTTTGGTGACACTTAACAAGGTTTTGTTTGTTAACAGTAGTTAAATATCTGTCATGTCATGGTTACGGCAAGGTTAGAAAGGAATAACGGTTAGTAATGTTATGCTCTGTTCACACCAGAAGCCGTTTGCGTGGATAAATTGCGCCATTCTCGCGTAAATGGACGTCAATTCATTTGAAGCCATGCCTGAGTCCACTAGATTCATTCTGAGATGCACCCAGCTCTGTGAGCTCATAAACACCTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36644
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 1072 | 4812 | 21 | 81 |
ENSDART00000100830 | Nonsense | 86 | 140 | 3 | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | Nonsense | 1011 | 1146 | 20 | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21117095)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21347318 |
GRCz11 | 18 | 21336384 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCGATGCTTCTCTGGTTCCACTATATGAGAGGCTTATTCTGAAGAGTT[T/A]GTCCTCCTTGAACCTCTCTATGGAACTGCTAGTGCACGAGCCCTTTGGAT
Long Flanking Sequence:
AGCATTTGTTTTAAAAACAAAATGCAGCCAAATGTACTTCTGGCTACATAATTCGTAATCTCCAAAAATTTATATAAGGTTATATTTTTCAGAATGAGCTCATGTTGAAAACATTAATGGCAAGGGCCATCAAAGAGTAGTCCAAAGTCCAATCTCAGTTCTACCCCTTATCCCTTCCCCTTTCCCCTACCCCTCATTTTGCGCATTCCCGTGTAGGGGAGGGGTTGTCCCAATTCTCTTTAACTTGAAGGTGTATCGCTAAATGGTAGGGGTGACAAAGATATAAATTTCTTTATTCAAAGTTTGATTAATTTAATATGTCATTCAAAAAAATTTAATCATTACAAACCTTACTAACCCCAAATTTTAAGAGTATACAAGATAGTATAAAGAATACTTTTGTTATGTTTTTTTCTTCAATATATTCATGAAGTTGTCTGACTCACAGGCTCCCGATGCTTCTCTGGTTCCACTATATGAGAGGCTTATTCTGAAGAGTT[T/A]GTCCTCCTTGAACCTCTCTATGGAACTGCTAGTGCACGAGCCCTTTGGATTGTGTGATTATGATGGGGATGATCTGTCTACAACCTCAAAGGTAAACAGTCTGATAGTCACCGGTAATGGCATGGTAATTGGATTTTAAGTGGGAACCATTACTCATTACTTCATTACAAGCAATACAAATTTATATAATGATTGTAGGTTTATCTGAATGTTGCACATCTAAAGGTTGCTTTAGGGCTAAACACACCCGTATGCTTTGGCACAGCCTGCGCATGTTCGTTTAGCCCTTGTCGTGGCTGACACCAACACTGATGCGCACCTCTCAAACAATGTAACTACACGTCGCAATGTGTAGCGCAAGCTCTGTGATTGGTCAGCTTGGTAGCGCTGACGAGTGTGGGCGGGACCGAGGGCCGCGCGAACCTGTTGGAGCGAGTGTTTAAAAGTGTTGAGTCCTGTGAAGGAGCTCCAGATATTAATAATAATACATTTTATTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12926
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 1195 | 4812 | 22 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | Nonsense | 1134 | 1146 | 21 | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21119089)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21349312 |
GRCz11 | 18 | 21338378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGCAAGCTCACTATGACCAACTGYAGCCCACKCTGCGTTTCATATCGTT[G/A]GGCCTTCCTGGTGGACCAACAACAGTGCCATAYTGGGTAGGAACAGCAAT
Long Flanking Sequence:
GCATCAGCTGAATAAAACATATGCCAGAATAGCTGGCGGTTCATTCCACTGTGGTGGACCTTATAAATGATGGAATAAGCGAAGGAAAATGAATGAATGAACGAATGAATGTTGCACATCTACACATGCAAGTGTGCATGTAAGATTTTTATTGTTTTACATTACTATGACCCGAGTACCTGAATGTTTGGTCTTTTAGTCTAATAGTTTTTGTCTTCTGTAGAGTCTGGTGTTGGCCGTTGGAGCTCAGCAGGAGTTATGGGTCCGTTTCAACCCCATGTATCAACAGGACTGCCACAGCCGTGTGGTTGAAGAAGTGCTGGAGTTCTGCTACCATGGCCATCCTCAGCAGGACAGGGTGTTGCTGAAGGGAGAGGTCCAGTTCCCAAATCTTAAGTTCTCCAGCACTACACTAGATTTCGGCTGTATTCTCAACAACACAAAATCACGACGCAAGCTCACTATGACCAACTGCAGCCCACTCTGCGTTTCATATCGTT[G/A]GGCCTTCCTGGTGGACCAACAACAGTGCCATATTGGGTAGGAACAGCAATTTTACATTTTTGTTCCGTACGGCGAAAGCCTCAAAAACAACATGGCTTTCATTGCTTGGATAAAAAATTCTGTGAAACATTTTTCAAAAGATGATAGAGTGCTTCCTTATCTGATGTTTAGTCAATTGGCATAAGCTAAAACAGTTAGAAGCATTTCTTTGCAAAGTAAACTTGGCTGTTCTGTGCTTTAATTTCAAGCCAGTGCATTTTCAATGTATCCCACCAAAGAAAAAGGGCCCTACTGCATGGACCTAAGCTGATATTTAGCAATTCAAAGGCTGCATAAGCGACCTCTTGAAAGATATGTTCAAGGAGTATTGATTTCCTGTTGACAAACAACAACAAAAAATAAATAAATAAATAAACTTGGGGGAATTAAAAGACTCTTCAAAAGCCTCTAAAGATTAAGAAATCGATGCCTTGCTTCAGCACTCAGATGTTAAAGATGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43101
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 1279 | 4812 | 24 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21125166)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21355389 |
GRCz11 | 18 | 21344455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCATCATGGTAGCTCCAATGGAAATGAGCAAAATAGGACCTGCTTAACA[C/T]GAAGAAGCAAAGAGCTGGGAAGCAAACCCATCAATCTCACAGCCAACGGG
Long Flanking Sequence:
CATTTTTTGATTAACACTGCCCCCTGCTGACTGCATTTATAACCACACTCGCTGTTACAACCTACTTATCTTCAATACTTTTATTTTAGTCAGTTTTTTCAAGATTTTTTATTTGCTTTCTTCCTTGAAGGGATATATAATATTACACACTGATTCCATCAATGCCTAGTCTCTGTATGGCTCTTATTGTATTCTGTTCCCTTTCTTTAGAGCCTGAGATTTCCTGTGTGATCTTTTCCACTGATCAATTACACCCATTCAATTATTTAGTGCTTTCTGTAATGAATGGCCATCTTCACAGACCCAATTTGGTTTCCGCCTGACCCTTTAGGCGGAACTAGAATGTGGAGTTAGATGGAGATGATTGGTGAAAACCCCTAATAATGTGTCATTGTTTATGTTTCGGCAGGGAGACTGACGTAATCATACCTCAATTGGAAGAGGAAGAATTGCATCATGGTAGCTCCAATGGAAATGAGCAAAATAGGACCTGCTTAACA[C/T]GAAGAAGCAAAGAGCTGGGAAGCAAACCCATCAATCTCACAGCCAACGGGCATCCGAGTGTGGGTGTGAAAGAGGTTGGTTTAAAGCCCAAATATACTACAGTTTTTTTTAACATATGTTTATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCTATACACTTTTGTATAGACGTGTCTTGAAAAATAACTAGTAAAATATTATTTACTGTCATCATGGCCAAGATAATTTAAATCAGTTATTAGAAATGTGTTGAAAAAGTTTTCTCTCCATTAAACAGAAATTTAACGGGGGCTAATAATTCAGGGGAGCTAATATTTCTGACTTCAACTGTATATCTAAAGTGCACTTGTGGGTTCTATACCTTTTTGTTGACATTCTATTCTTTAAAGACTGACTTATTATCTACTTGCATTTAAATTTCCTTTTTTTACATTACAATCATACTCTTGTGTTTGAAGGTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12486
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Essential Splice Site | 1303 | 4812 | 24 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21125242)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21355465 |
GRCz11 | 18 | 21344531 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCCATCAATCTCAMAGYCAAYGGGCATCCGAGTGTGGRTGTGAAAGAGG[T/C]TGGTTTAAAGCCCAAATATACTACAGTTTTTTTNNACATATGTTTATAAA
Long Flanking Sequence:
ACTTTTATTTTAGTCAGTTTTTTCAAGATTTTTTATTTGCTTTCTTCCTTGAAGGGATATATAATATTACACACTGATTCCATCAATGCCTAGTCTCTGTATGGCTCTTATTGTATTCTGTTCCCTTTCTTTAGAGCCTGAGATTTCCTGTGTGATCTTTTCCACTGATCAATTACACCCATTCAATTATTTAGTGCTTTCTGTAATGAATGGCCATCTTCACAGACCCAATTTGGTTTCCGCCTGACCCTTTAGGCGGAACTAGAATGTGGAGTTAGATGGAGATGATTGGTGAAAACCCCTAATAATGTGTCATTGTTTATGTTTCGGCAGGGAGACTGACGTAATCATACCTCAATTGGAAGAGGAAGAATTGCATCATGGTAGCTCCAATGGAAATGAGCAAAATAGGACCTGCTTAACACGAAGAAGCAAAGAGCTGGGAAGCAAACCCATCAATCTCACAGCCAACGGGCATCCGAGTGTGGGTGTGAAAGAGG[T/C]TGGTTTAAAGCCCAAATATACTACAGTTTTTTTTAACATATGTTTATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCTATACACTTTTGTATAGACGTGTCTTGAAAAATAACTAGTAAAATATTATTTACTGTCATCATGGCCAAGATAATTTAAATCAGTTATTAGAAATGTGTTGAAAAAGTTTTCTCTCCATTAAACAGAAATTTAACGGGGGCTAATAATTCAGGGGAGCTAATATTTCTGACTTCAACTGTATATCTAAAGTGCACTTGTGGGTTCTATACCTTTTTGTTGACATTCTATTCTTTAAAGACTGACTTATTATCTACTTGCATTTAAATTTCCTTTTTTTACATTACAATCATACTCTTGTGTTTGAAGGTGTTTGATATCTCATCACTTTATGGGGTATTAGAACCTGGTGACAGCAAGCTGGTGACCTTCTCATTTCTTGGTCATGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39199
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Essential Splice Site | 1886 | 4812 | 36 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21140721)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21370944 |
GRCz11 | 18 | 21360010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTGTGGCAGAATTCAAAGGTAATCTAAAAGTTCTCACCTCTTTTTTAA[G/T]AATCCACAGAAGGTCTTGCAGAAGGAGACAAGGGGGAAACAGATGCACTA
Long Flanking Sequence:
CCAGATTATGTTTAACAGAGCTAGGAAATTTTCACGGTATGTCTAATATTTTTTTTTTTTTCTGGAGAAAGTCTTGTTTTATTTCAGCTAGACAAAAAGTAGTTTTTAATGAAAAAATAAAGCATTTTATTCTGCGTAGAAACGTGCTGGATAATTTGGCGGTTCATTCCGCTGTGGCGACCACGGATTAATAAAGGGGCTAAGCCGACAAGAAAATAAATGAAAATATAATTTACTGTCATCATGGCAAAGTTCAAATAAAACAGTTATTAGAAATGCGTTATTAAAACTATTATATTTAGAAATATGTTGAAAAAATTGCCCTCCATTAAACAAATTGGGGAAAAAATAAACAGGGGGGTTAATAATTCAGGAGGGCTAATAATTCTGACTTAAACTGTATATGATTAAAAAAAAAATTTTCGATGGACATTCACATTAAAGGGTTTGGCTTGTGGCAGAATTCAAAGGTAATCTAAAAGTTCTCACCTCTTTTTTAA[G/T]AATCCACAGAAGGTCTTGCAGAAGGAGACAAGGGGGAAACAGATGCACTATTTGAGGGTGAAATACCCGGTGTTAATGGTAAGCTTTAACCAGCGGGAACAGTAATTTCATTGCATTCATCAATGAGGCTGTTATAAAAATTCAGTAATTATTTCACATATATAAACACGTATTCCCTTACAGGCTTACCTAAGGGCAACAGCAGTGTTGTCACTGCAGTGGGGGATTTGGAATATGACCCTGTATCTACAGCTGTCGCACGTTACATGGGCATCGATCTTTCACCAGAGGGTAAAGCTGCACTGAATCGCCGGGGCATTGCCATCATTGTGCACGGCGCTCCTTTATCAGGTAAGAGTTGACGAAAATCTTTTTTTGGCATGAAGATTTTTGGAAATAAAGATTTTAAAAATGTTTTTTAATGACATCCATTCTGCTCACTAAGACTGCATTTATTTAAAAATAAAAATAAATAAAAAAATTTATATCAATTATATAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43102
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 1929 | 4812 | 37 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | Nonsense | 18 | 268 | 1 | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21140957)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21371180 |
GRCz11 | 18 | 21360246 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACCTAAGGGCAACAGCAGTGTTGTCACTGCAGTGGGGGATTTGGAATA[T/G]GACCCTGTATCTACAGCTGTCGCACGTTACATGGGCATCGATCTTTCACC
Long Flanking Sequence:
TGTCATCATGGCAAAGTTCAAATAAAACAGTTATTAGAAATGCGTTATTAAAACTATTATATTTAGAAATATGTTGAAAAAATTGCCCTCCATTAAACAAATTGGGGAAAAAATAAACAGGGGGGTTAATAATTCAGGAGGGCTAATAATTCTGACTTAAACTGTATATGATTAAAAAAAAAATTTTCGATGGACATTCACATTAAAGGGTTTGGCTTGTGGCAGAATTCAAAGGTAATCTAAAAGTTCTCACCTCTTTTTTAAGAATCCACAGAAGGTCTTGCAGAAGGAGACAAGGGGGAAACAGATGCACTATTTGAGGGTGAAATACCCGGTGTTAATGGTAAGCTTTAACCAGCGGGAACAGTAATTTCATTGCATTCATCAATGAGGCTGTTATAAAAATTCAGTAATTATTTCACATATATAAACACGTATTCCCTTACAGGCTTACCTAAGGGCAACAGCAGTGTTGTCACTGCAGTGGGGGATTTGGAATA[T/G]GACCCTGTATCTACAGCTGTCGCACGTTACATGGGCATCGATCTTTCACCAGAGGGTAAAGCTGCACTGAATCGCCGGGGCATTGCCATCATTGTGCACGGCGCTCCTTTATCAGGTAAGAGTTGACGAAAATCTTTTTTTGGCATGAAGATTTTTGGAAATAAAGATTTTAAAAATGTTTTTTAATGACATCCATTCTGCTCACTAAGACTGCATTTATTTAAAAATAAAAATAAATAAAAAAATTTATATCAATTATATAACATTTTTTTAAATAACTGCTTTTTTTATTTAATGTAGTTTAAATTTGCTGAATGCTGGAATTGAAAATTAAATGATTAAATGTACTGTAACAATGAATTTGCTGAATGCTGGAACTGAAAATGCCTTATTGTAGCATCATCACTTATTATTGAAATTAATATGATGATCTTTTACTCAAGAATTATTATAATTATGTCTTGAAAACTTTCCCAGAGATGGGTTGCGGCTGGAATCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36645
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Essential Splice Site | 2089 | 4812 | 38 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | Essential Splice Site | 178 | 268 | 2 | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21143108)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21373331 |
GRCz11 | 18 | 21362397 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGGACGTTCACAGAAGAATGACAGCTCCAATCCTGCTGCCTCAGTGG[T/C]AAACACTTATTAATTTGGCACATACAATACACACAGTAGTAGAGGTAAAA
Long Flanking Sequence:
TTCCCATTTGTACATTTATTACTGTAAGCAAATTCAGTCTTGGTGAGCACAACATGGAACATTTTAAACATGAAAAAAATCTTACTGATCCCAAAGTTTTGTCCGGTGATGTGCATGTAAACGTCTGTGTGCAGGTAAAACAAGAACATCAGTTACTCTGGCAAAACACTACGGGGCAGCATGTCTCAGTGTGGATGAGGTGGTGCAGGAGGCTTTGTCATCAGGGAACAGTTCTGCAGCCTGGAGGGCAAGAGAACTATGTGCCAAGGCTGCAGTGGTGTTTGCTCAAAGGGAAGAGCAGGAGGCAACGGTGGATATTACTGCCACTGCTTCTCAGGCTGCTGGTGTCCTAAGTATGGAGGCTGTTGCCAAACACACAGCAGAGGGCAGCCAGATCAGTGATCTAAAAGTTCCCCCGTCATCGGCCTCAACCCGAAATAAAACAAATATCACAGGACGTTCACAGAAGAATGACAGCTCCAATCCTGCTGCCTCAGTGG[T/C]AAACACTTATTAATTTGGCACATACAATACACACAGTAGTAGAGGTAAAAAGTCTATTCACTCAGTATTGTTCTAGTAAAATCACATAAATACAATATCAATACTTGAAGCAGCACTGCACTTTATAAAAATAATAAATTATAAGGTCATACTGGAATTAATCTAAGAGGTTCCAATAACAGTATGAAAATAAATGATGTACCAACAGGGTAAGAAAAAAGTATTTCACTAATGAATTATCTTTTTAAAATAATATTAATTATAAGAAAATATAATACTTGTATATTAAAATGCATTACTGTATCTACTACATGTGCTTTTTTTTAAAGGGTTGGTAAGTAACATATTTATATAATAATAATAATCATATATGAAAATGTCAAAATATTACACTTAATAACTGTCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACATGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43103
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 2216 | 4812 | 41 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21147573)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21377796 |
GRCz11 | 18 | 21366862 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCAAGAGAAGAGCAAATGACTCCTAGTGAAGATTGGGATACCACCCCA[C/T]GACCTGAAGACCCTGTGCCCCTCTCTGAGGATGTAAAACAAGAGCTGGTT
Long Flanking Sequence:
ACAAAAACTGCAAAAAATTGTACCTCCTGGAACCTATTTTGCGCTCTCCAGAAATGTATACAGGGGTATGTATTTATAATGAGCCTGGGTTGCAAATAACAGTATTTATTTTTTTTTTATGTATGTCATAATAAAGATGTTTTTGAAGCTAGTTTTTTTATCCAACACTGTCAGAAAGAAAGGTACTGATATGGTACTGATATGTATCTTTATTTCTAATTTAAATAAGCTTTCTGTGTATCCTGTATAAGGAGTTATGAATATTTTAAAAACAGGTTAACTAAAATAGTAAGCAAATTCTGAATTATTAATCATAGGATGCTCAATAGTTCTTCTTTATCTTATTCAATGAAACCTTGTGAGAATGAATTATTAAAATTGTGTATTACTTTAGAGAAAAGCACAAACTTGACCAAGAACAAGAAGCGAGAATTCAGTGGGAGCTGGAGAATTCAAGAGAAGAGCAAATGACTCCTAGTGAAGATTGGGATACCACCCCA[C/T]GACCTGAAGACCCTGTGCCCCTCTCTGAGGATGTAAAACAAGAGCTGGTTAGTTTGAGTGTGCATTTCATAATATGCTTGGTAATTTTCATACATGAAATAAAGTTCCAGTGAGTTCCGATCAAGTTAAAGTGTACACCTTATGTTGAAGCAATTATTATACCTATTATACAAAAGCTAAAATCTGTTTTAAAAGCCTTTGCTGTAATTGTTATTCCTTATTAATAGTCCATTGAGAGTGACAGACATCTGCAGGTGCGATTTCATCAGTACGAACAGAGCCAAGCAGAAATACAGCACATTCTTCAGTTCTGGGACCGAACGCAGAGTCGTTTATTGCAGCCAATGGTGTCTGAAGTCCAGGAGACTGTAGACATCACCGATTGTCCTCCATCTTCTGCAAAGAAGACCAAGAAGGAACGAGAAAAGGAGAAAGCTGAGAGGGAAAAGTTAAAGGTTGATTCTGAAACTAAGTCACAAACTCTTAGCCAGACCCAAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29030
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 2296 | 4812 | 42 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | Nonsense | 65 | 161 | 1 | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21147993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21378216 |
GRCz11 | 18 | 21367282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGACATCACCGATTGTCCTCCATCTTCTGCAAAGAAGACCAAGAAGGAA[C/T]GAGAAAAGGAGAAAGCTGAGAGGGAAAAGTTAAAGGTTGATTCTGAAACT
Long Flanking Sequence:
AAGAAGCGAGAATTCAGTGGGAGCTGGAGAATTCAAGAGAAGAGCAAATGACTCCTAGTGAAGATTGGGATACCACCCCACGACCTGAAGACCCTGTGCCCCTCTCTGAGGATGTAAAACAAGAGCTGGTTAGTTTGAGTGTGCATTTCATAATATGCTTGGTAATTTTCATACATGAAATAAAGTTCCAGTGAGTTCCGATCAAGTTAAAGTGTACACCTTATGTTGAAGCAATTATTATACCTATTATACAAAAGCTAAAATCTGTTTTAAAAGCCTTTGCTGTAATTGTTATTCCTTATTAATAGTCCATTGAGAGTGACAGACATCTGCAGGTGCGATTTCATCAGTACGAACAGAGCCAAGCAGAAATACAGCACATTCTTCAGTTCTGGGACCGAACGCAGAGTCGTTTATTGCAGCCAATGGTGTCTGAAGTCCAGGAGACTGTAGACATCACCGATTGTCCTCCATCTTCTGCAAAGAAGACCAAGAAGGAA[C/T]GAGAAAAGGAGAAAGCTGAGAGGGAAAAGTTAAAGGTTGATTCTGAAACTAAGTCACAAACTCTTAGCCAGACCCAAGTGTCAACAGATGGTGTCGAGGGCTTGGAAAAAATAGTGCTTCCAGAGCCTACTCCGCACACATGGATGTCTCTGAAAGAGAACAAAGAACTGAGCGCATTTGAGATCATCAAAAGCATGAAACTACCCTCCCATGAGGAGGTAAAGTACTTTAGCTTCTTTTTATGGTAATGTTTTGTTGAAAGCAAGTATGAGCAATATTAAGTCCATTTATTTTGTTTTATTTAGATTTTGGATGAGTTAGGGATAGGACCTAAAGGTCCACCCATCCCACCACCTATAATATTCTCCATAGTCCATTACCCTAAGATGAGACCACCCAACACACAGCTCTCCAGCAACTACTTTACATTTTTGAAGCCCATATCTTGTGAGGACCTGTCAGAGAAAGAAAAAGAACTCGGATCAGAAACTGTCAAGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43104
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 2420 | 4812 | 43 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21148453)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21378676 |
GRCz11 | 18 | 21367742 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAGCAACTACTTTACATTTTTGAAGCCCATATCTTGTGAGGACCTGT[C/A]AGAGAAAGAAAAAGAACTCGGATCAGAAACTGTCAAGGTACTAAAATATC
Long Flanking Sequence:
CGATTGTCCTCCATCTTCTGCAAAGAAGACCAAGAAGGAACGAGAAAAGGAGAAAGCTGAGAGGGAAAAGTTAAAGGTTGATTCTGAAACTAAGTCACAAACTCTTAGCCAGACCCAAGTGTCAACAGATGGTGTCGAGGGCTTGGAAAAAATAGTGCTTCCAGAGCCTACTCCGCACACATGGATGTCTCTGAAAGAGAACAAAGAACTGAGCGCATTTGAGATCATCAAAAGCATGAAACTACCCTCCCATGAGGAGGTAAAGTACTTTAGCTTCTTTTTATGGTAATGTTTTGTTGAAAGCAAGTATGAGCAATATTAAGTCCATTTATTTTGTTTTATTTAGATTTTGGATGAGTTAGGGATAGGACCTAAAGGTCCACCCATCCCACCACCTATAATATTCTCCATAGTCCATTACCCTAAGATGAGACCACCCAACACACAGCTCTCCAGCAACTACTTTACATTTTTGAAGCCCATATCTTGTGAGGACCTGT[C/A]AGAGAAAGAAAAAGAACTCGGATCAGAAACTGTCAAGGTACTAAAATATCAAAAAATTTAACAAACATAAAAGTAGGACTGACTGGACTGACTCACTGACACCAAACAGGGTTGACAATTACTATTATGTTGACAAATTCATTTGACTATAACAAATGCTCTCCAATTACAACAGATCTGACAAAACCCAACAAATTGTCTACTGTTATTGACCTGTTGGTGAAGTCTGAGTTGGCCGTTATACAGTTAGGTCCATAAATATTTGGACATTGATACAATTCTAATATTTTTGGCTCAATACACGAACACAATCGATTTGAAATTAAATGAACAAGATGTGCTTTAACTGCAACCTGTCCGCTTTAATCTGAGGGTATTTACATCCAAATCAGGTGAATGGTTTAGGAATTACAGTAGTTTGCATATGTGCCTCCCACTTGTTAAGGGTCCAAAGGTAATTGGACAATTTTTTCTTTTTTTTATGACTACACCAGAGTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8483
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Essential Splice Site | 2456 | 4812 | 44 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21150032)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21380255 |
GRCz11 | 18 | 21369321 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATCCAACCCTGGCCAGTCTGAGGAGCCCAAMCCAGAATATAACCAAGGG[T/A]ATARGAGATTCCYTATGCAWATRAAAGCATKTAAAATCACWAATAAATAG
Long Flanking Sequence:
GGCTGGCAGAGCCCCACTATGAATGAAACCCAGCGTCTGGTGATGTCTATGCGTTTCAGACTTCAAGGCTGTTATTGACTGTAAAGGATTTGCAACCAAGTATTAAAAAGTCAAATAATCATTTGATTTATGATTATTATTTTGTCCAATTACTTTTGGACCCTTAACAAGTGGGAGGCACAAATGCAAACTGTTGTAATTCCTAAACCATTCATCTGATTTGGATGTAAATACCCTCAAATTAAAGCGGACATGCTGCAGTTAAAGCACATCTTGTTTGTTTCATTTCCAATCGACTGTGTTAGTGCATAGAGCCAAAAATGTTATAATTGTGTAGATGTCCAAATATTTATGGACCTAACTGTATATTTTGGAATAATTTGAATAAGAAAAAAAGAATACTTGTTCAATTTCATGTTGCTTTGTAGGAGGGCATGACAATTACTACCACATCCAACCCTGGCCAGTCTGAGGAGCCCAAACCAGAATATAACCAAGGG[T/A]ATAGGAGATTCCCTATGCATATGAAAGCATTTAAAATCACTAATAAATAGAAGCCTTTACCTACAGTACAGTATGTTTTAAATTTGTTCTTTTGCAGACTCACTGATTTCCGTTGGATTGTACCACCAAATGGAGCCATTACCCTAAGGATCAAGTTTAACTCTTCAGTTCATGGGCAATTTCATCAGACTTTCAGCTTTGAGGTCTTAGGGACCAAACGATGTTATCAGCTACACTGTAAAGGAATTTGTACTTACCCATCGATAAGCCGAGACCCCAAGTGAGTGACATTTCAGTAGGGAAATATACTGTAGTTATCATTGCCATTGGACATGTAGAACTTAGTAGCCTTTTTTGTGTGTAATAGGATTCTGTTTGCCCACTGCAAAAAGACACTGCGTCCTGAGAGTGGACTACAGAAGACTTACGTTATCCAGTCAGACCTGTATGAGTTTGGACCTCTCCTATGTGGAAAGACCAGGGACAGGTGCTAGCATCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17202
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 2524 | 4812 | 46 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | Nonsense | 69 | 1388 | 2 | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21150419)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21380642 |
GRCz11 | 18 | 21369708 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAACTTAGTWGCCTTTTTTGTGTGTAATAGGATTCTGTTTGCCCACTGC[A/T]AAAAGAYACTGCRTCCKGAGAGTRGACTACAGAASACTTACRTTATCCAG
Long Flanking Sequence:
AGAAAAAAAGAATACTTGTTCAATTTCATGTTGCTTTGTAGGAGGGCATGACAATTACTACCACATCCAACCCTGGCCAGTCTGAGGAGCCCAAACCAGAATATAACCAAGGGTATAGGAGATTCCCTATGCATATGAAAGCATTTAAAATCACTAATAAATAGAAGCCTTTACCTACAGTACAGTATGTTTTAAATTTGTTCTTTTGCAGACTCACTGATTTCCGTTGGATTGTACCACCAAATGGAGCCATTACCCTAAGGATCAAGTTTAACTCTTCAGTTCATGGGCAATTTCATCAGACTTTCAGCTTTGAGGTCTTAGGGACCAAACGATGTTATCAGCTACACTGTAAAGGAATTTGTACTTACCCATCGATAAGCCGAGACCCCAAGTGAGTGACATTTCAGTAGGGAAATATACTGTAGTTATCATTGCCATTGGACATGTAGAACTTAGTAGCCTTTTTTGTGTGTAATAGGATTCTGTTTGCCCACTGC[A/T]AAAAGACACTGCGTCCTGAGAGTGGACTACAGAAGACTTACGTTATCCAGTCAGACCTGTATGAGTTTGGACCTCTCCTATGTGGAAAGACCAGGGACAGGTGCTAGCATCTAGTACTTTTGCATTAACGGTCATCTTTCATGTTTAAGATATTGCATAGGAATGTAAGTGTATATTTGTTTTTTATTAATATTATGATGTTATCCTGATTTAGATATAAAGAAGGAAAATATCCAGAGAACATGGAAAAGTTTGTAATTCACAACAATTCTCAAATGGATGCAGAGATCCAGTTTTGCTTTCAACATGACAGCAAGGCCACGACTTTCCTTCTTGACCCTCCAAATATGACCTTGAAGACCAATGAGCGAAAGGTATGAGCGTTTATACTTTGTACTCTTTATCTTTTTTGTACTCTTTTTATACTTTGGACTGTATGTGGGATACAGTACATGCGCTGATTATTTGAATAAGCTAACATTTGGACAGCTGTTACCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25063
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 2794 | 4812 | 51 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | Nonsense | 339 | 1388 | 7 | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21154040)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21384263 |
GRCz11 | 18 | 21373329 |
KASP Assay ID:
554-7447.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACATTCAAAGTGTCAGAAGAAGTCAAGCGGTCTATTAAGTTAGAAAAC[A/T]AGGGCAAATATGACATAGCATTTAAGTAAGTTATGTAGATATTTAATCTT
Long Flanking Sequence:
TGCTATTTATACAGAAGGAATTATCCACGCACAATATGAATTCCCAATTAGAAAAATACTACAAACTAAAATATTACTTATGAAAAGACCTAAATAACAGAAATGTCCAGTACAAGCGAGCTGTATTCCAGACTAGTTCCGCCCGATGACGTAATGTCTCTGACACCACCTGTAGTCCCGTTTAGCAACTTGATAGCAATCATCTTTTTAAAGAAATGTAACCGTTTTTAAAAATCAAGAGTTGGATGTAACTGATGTGTTTTATGTCGTGGAATGAAACGTGAAAGTATCTTGAGTTTGTGGAAGCTACAAACCATATTTAAGCTAATTAACCAAAATCCCAGCTTCTGGGTTTTTGCATACAAATTGACGTCATAGTTCCTCCACTCTATTCTTTTGTTCATTTAATGTTTGTATTTACTGCAGATTTGGATGGGTCATTAGACTTTGGAACATTCAAAGTGTCAGAAGAAGTCAAGCGGTCTATTAAGTTAGAAAAC[A/T]AGGGCAAATATGACATAGCATTTAAGTAAGTTATGTAGATATTTAATCTTACATTACAGTTTTCGTGATGAGATATTATCAAATATGTCTGTATACGTCCTCTCCTTTATAGGTTTACATTAGATGCGACAGAGCCAGGAATGCCGGATCTGAACTCAATATTCTCCATCACTCCTCGGAAGGGCTCTCTACGCCCCAACAATAAACCCACCACTGTCCAGATTATTTATCAAAACGACAAAGAAATGTCCATCAGAGATAGCCCAATCCTTTGTTGTCAGGTATTTTATAAATTAATACATTCTTTGCAATCCAATTCAGTACTCAGTTACCATGATTTGTTTTTTTATCTTAGCTCTGCTGCCATCAGAGACCAATGTTTAGTATTTTTCCCAGGTTATTGAGCCCAATTTGGAGGGAGGCGAGACCATTAGTACTATTCCAATCAAAGTGTCAGTCCAGGCAGTTTTCTCCAAGTACATTATCAGTCCCTCTAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43105
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 2842 | 4812 | 52 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | Nonsense | 387 | 1388 | 8 | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21154271)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21384494 |
GRCz11 | 18 | 21373560 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGCTCTCTACGCCCCAACAATAAACCCACCACTGTCCAGATTATTTAT[C/T]AAAACGACAAAGAAATGTCCATCAGAGATAGCCCAATCCTTTGTTGTCAG
Long Flanking Sequence:
AAATCAAGAGTTGGATGTAACTGATGTGTTTTATGTCGTGGAATGAAACGTGAAAGTATCTTGAGTTTGTGGAAGCTACAAACCATATTTAAGCTAATTAACCAAAATCCCAGCTTCTGGGTTTTTGCATACAAATTGACGTCATAGTTCCTCCACTCTATTCTTTTGTTCATTTAATGTTTGTATTTACTGCAGATTTGGATGGGTCATTAGACTTTGGAACATTCAAAGTGTCAGAAGAAGTCAAGCGGTCTATTAAGTTAGAAAACAAGGGCAAATATGACATAGCATTTAAGTAAGTTATGTAGATATTTAATCTTACATTACAGTTTTCGTGATGAGATATTATCAAATATGTCTGTATACGTCCTCTCCTTTATAGGTTTACATTAGATGCGACAGAGCCAGGAATGCCGGATCTGAACTCAATATTCTCCATCACTCCTCGGAAGGGCTCTCTACGCCCCAACAATAAACCCACCACTGTCCAGATTATTTAT[C/T]AAAACGACAAAGAAATGTCCATCAGAGATAGCCCAATCCTTTGTTGTCAGGTATTTTATAAATTAATACATTCTTTGCAATCCAATTCAGTACTCAGTTACCATGATTTGTTTTTTTATCTTAGCTCTGCTGCCATCAGAGACCAATGTTTAGTATTTTTCCCAGGTTATTGAGCCCAATTTGGAGGGAGGCGAGACCATTAGTACTATTCCAATCAAAGTGTCAGTCCAGGCAGTTTTCTCCAAGTACATTATCAGTCCCTCTAATGATATCAACTTTGGCCCAATGGTTCATGGCTCACGTAAAAAACAGACTCTCACTGTGGAGAATAAAGGCAACTTCGAGATGCGGTTTACCATTAGGCTGTGTAAAAACGCCTCAGTTCCTGCACAGAGGAGAGGGTACTGCATTTTTTATTAAAAAATTGTATATATGTATTCAGTTGAAGTCAGAATTATTAGCCCCCCTGTATACCCCCCCCAAATCCCCCCTATATAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16299
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | None | 3230 | 4812 | 58 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | Splice Site, Nonsense | 775 | 1388 | 14 | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21158691)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21388914 |
GRCz11 | 18 | 21377980 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGGCAAACTCTTCCATTAGTGATCAAGAACAACAGCAATGTGCCTGCA[C/T]AAGTAAGATAAGAATTTGTTTGACTAAACTACAGTTTATATGACTTTCAA
Long Flanking Sequence:
TAAAAAAAGCATCAAAAACACCTAATTTTAAAAAATATGATTGAATGCCACATATCTCAAAAATAAAATCTGATTTTATATAATCATATACTTGATTAATTTAAATCATTTCTAAAGTGAAGAACAGTAACTTATTTGGCCCAAGCTATTTTTTAGTCCCACACTTTTTTTTCACCTAAAAGACACTGTATTGGTGAATCCGGGTTTGCTCGTTCTATACCAGGTTATTGTTTTCAATGTATATTTGAACTGCTTGGATGCTTGTTGAAATTTTGTTGTGGCTTTTCTCATTCTCTTTTGTCCAAAGTCAAGTATCTGCCCACAGACCCAAAGCTCTGGTGTTTGATCTAATGGGTGAAGGCAACTTGCCCTGCATCACTGTTTTAAAACCTGTTCAGAGGACTAATCAAGGTCATCCAGTGCTACAGTTTAAGCGCTCATTGGTGGGACGAGGGCAAACTCTTCCATTAGTGATCAAGAACAACAGCAATGTGCCTGCA[C/T]AAGTAAGATAAGAATTTGTTTGACTAAACTACAGTTTATATGACTTTCAATATTCAATGGAATAATGTATTGTTTAATTTTCAGGTTAGCCTTATTTTACAATATCTCCCAGACGTTTTTACTCTAAAAGCTGCTCCTGGAACTGTATGCCGACTAGCCTCCTCACACATTGAAAGTGATCCTGGAAAAGGCAAGCCATTAAACTCAAATAAAATGTGTTCCCACTGCCTCTACATTAATTTCTCTCCAAATAAGAGAATTAAAACCATCAAAAGCAGCAGGATTTTTTCGTTAAATTGTTTGTCATTTGATTATTTAGGGGGTGCTTCGAGCCACAAAATACAGTGTGATAGGTAACTTCACATCAAGCTGTTGTGTTTGTCCAGTAAAATACAGTCAGTGACCAATCAGATTTGTGCATTCTGGAAAGCTGTATATTAACTTTAAATTTTAATTAAGTCATTTGAAGCTTTATGGTCATTGCATTTCGCAGAGTGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12927
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 3337 | 4812 | 60 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | Nonsense | 858 | 1388 | 16 | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21159569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21389792 |
GRCz11 | 18 | 21378858 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGTTACCATGACATTATCATTCTGGAGAACGTTGGCAACAGAGTTCAG[C/T]AGGAAAGCACTGAAAGTAAGTGACAATGAATTTTTCAAACATTCTAAAGC
Long Flanking Sequence:
TTTGTCCAGTAAAATACAGTCAGTGACCAATCAGATTTGTGCATTCTGGAAAGCTGTATATTAACTTTAAATTTTAATTAAGTCATTTGAAGCTTTATGGTCATTGCATTTCGCAGAGTGCAGCAAGAGAAGGAACAAACCGTTATTTTTTTATGACTTGTGTATAAACATTTAGCTCGCGGCAGGCAACCATAAGCAGTAAATTGAAATAAACAGAACGTTAGCATGAGATATCCAACACAAGTGTATTAAAATTAAATGTATGTGGCATTTTTTGCTTCTCTTCAGATGCACAGCTTGCTTATGTAGCCTCTTTGACACTTATGGCTGGCCAACAAGCTGAATTCCTGGTCGGGTTTCATCCGAAGGTGGCTCAAAAATTTGAAGCCAGCATGAAGCTAATGGTTAAAGATAACCAATATGATCAGACTGTGGTGCAGATTGTGGGTGAGGGTTACCATGACATTATCATTCTGGAGAACGTTGGCAACAGAGTTCAG[C/T]AGGAAAGCACTGAAAGTAAGTGACAATGAATTTTTCAAACATTCTAAAGCATAACTGAAATAATAATGGTGTCATTCATAACTCTGGTGTACTGTTGAGCATATTTTCATCCACTCTGGGATGTTTTTAAGTCTTATTTTGGCAACAACTTTCTCTGCTTTTCAGCAAATGGAAGGATTTTTGGTGACAAATCTTATTTTGACACATTGTTATTTTGGGAATATTCTTTGGAATTTTTAAAAAAAACTCAACTATACAATCTAGGCAAATTTATTAGCCTTTTCGTTTTGTTGGTGGCTATTTTGCCCAATTGGCTTCCTTTATAATAACATGTTTTGATTGGTAATTTTTAATTGTTAGCACCAATTGTTAATGGTGCCAATTAATGACTGTGGGGAAAAAAAAATATTTTTATAACTTTTGTGTATTTGTTTTTTATTAGAATTTTTTTGTTTGTTTTTCTTTTGTTTGATACCATATATTAACTAAACATACTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14679
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 4004 | 4812 | 71 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21170002)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21400225 |
GRCz11 | 18 | 21389291 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTCAGCTGTAGCTCCAGATCTGGAATTTTCTTCCCTCAAGCATAATTTT[G/T]GACTGCAATTCACATATTGTTCTGGTATGGTCCCTGCTACACACACACTG
Long Flanking Sequence:
CCAAATGTTGCAGCAGAAAAGTAAACTCATCAGACCAGGCAATGTTTTTCAATCTTCTATTGTCCACTTTTGGTGAGCCTGTGTGAATTGTAGCCTCAATTTTCTGTTTTTAGCTGGCAGGTCACTTAAATCGCCTTTCTTCCCCATTCTGATGCTCGGTTTGAACTGCGGCAGATCGTCTGATTAGAAATTGCCTTAACCAGCATTTGGACAGGTGTATCTAATAAAATGGCCAGTGAGTGTATTTGAAAAAGAAAAGAAAAGAAAAGCATTTGTTTGCGATGTAGTCATTTCCACATAGGCAAATGAATAGTAAATTCGAAAATAAAAAGATAATTTAGAAATTGCAGAATAAGATCAACAGTTTATTTACATGATTGTTCTGGTAATCACTTTCTTTCCTCTTTTTGTAGATAAAGAATGGTCCAATATTCTGTTGTGCCCTGATGGGTTCAGCTGTAGCTCCAGATCTGGAATTTTCTTCCCTCAAGCATAATTTT[G/T]GACTGCAATTCACATATTGTTCTGGTATGGTCCCTGCTACACACACACTGGTGATCAGCAACAGAAGCAGCAGTGCAATCAGGTAGATGATGTTCAACAGTTTTAAAAGTAAAATTGTATGTTTAGTTTTTATAACACATTGATGTTTATTCAGTCTAGACTGCTTGTTCTCCAACACAACCGTCCTGGAAGTGAACTTTACCCCTTTGGTCCTTTCTCCTGGTGGCTCTGTGGAGGTTCTTCTGTCATTCTACCCACGTAAAGCAGTTCGTTACCATGAGAAGGTGGTTTTTGAGATGAATAAGTGTGCAAAACGAGTTGTGGAGATCCTGGGACAGGGTGCTGAGATGAAGGTTATAAAAAGGGTTTGGTAGATTTAATACGATCTCATCGTTCGGATGTACAGCTATTCATCCTCCACTGTTTTTATTGTGGTCCTAGATTGATTTAGAGGACCCGGCACACAGAGTGGTCAATTTTGGAGCTTTGCAGATTGGCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43106
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 4114 | 4812 | 73 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21170492)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21400715 |
GRCz11 | 18 | 21389781 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATTGATTTAGAGGACCCGGCACACAGAGTGGTCAATTTTGGAGCTTTG[C/T]AGATTGGCCAGCAAAGTCGGAAATTGGTTTCCCTTGTGAATAACAGCCAC
Long Flanking Sequence:
GCATAATTTTGGACTGCAATTCACATATTGTTCTGGTATGGTCCCTGCTACACACACACTGGTGATCAGCAACAGAAGCAGCAGTGCAATCAGGTAGATGATGTTCAACAGTTTTAAAAGTAAAATTGTATGTTTAGTTTTTATAACACATTGATGTTTATTCAGTCTAGACTGCTTGTTCTCCAACACAACCGTCCTGGAAGTGAACTTTACCCCTTTGGTCCTTTCTCCTGGTGGCTCTGTGGAGGTTCTTCTGTCATTCTACCCACGTAAAGCAGTTCGTTACCATGAGAAGGTGGTTTTTGAGATGAATAAGTGTGCAAAACGAGTTGTGGAGATCCTGGGACAGGGTGCTGAGATGAAGGTTATAAAAAGGGTTTGGTAGATTTAATACGATCTCATCGTTCGGATGTACAGCTATTCATCCTCCACTGTTTTTATTGTGGTCCTAGATTGATTTAGAGGACCCGGCACACAGAGTGGTCAATTTTGGAGCTTTG[C/T]AGATTGGCCAGCAAAGTCGGAAATTGGTTTCCCTTGTGAATAACAGCCACTGTTCCTTGACTTTTTGTCTTCACAGACATTCTGATAACTCTCTTCACCACTCCAAGGTAAGTATGCGGTACAGTTTGTGCACATGGACACCATCATTCAAAAGTATAGGGAGTTGATAAGATTTTTGAAAAAGATTTGGGATAAAACATAAAGTTGACCATTAAAATAGAATTTATTTGATTAAGCATGCAGTAAGGCAGTAATATTGTGAAATACTATTACAGTTTTACTTGTTTTTCTATTTTAATGTATATTGTTGCTGTGATAGTAAAGCTGAATTTTTTGCATCATTAATCCAGTGTCACACGATCCTTCAGATCATCAAATCATTGTAATATGGTGATTTGGTGCTCAAGAAACATCTTTTTTTGTATTTTAATTCTGTGTTGAAAACAGTCTGGGGCTTTATTTTAATGATCTAGGTGCAAAGTCTAAAGTGAATGGTGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32205
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 4158 | 4812 | 74 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21171898)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21402121 |
GRCz11 | 18 | 21391187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACAATTTTTTTTTCTCCCTTCAGATCTTGTCAGTGCGTCCAGATGGC[C/T]AGGTAACACTTAAAGAGGGAGGTGGCCGCTGTGCGGTTGAGCTTCTCTTC
Long Flanking Sequence:
TTCAAAACTACTTTAAAATGTAAACTTCGCAAAATGTAAAAATTTTAGTTTTTATGGTCTAAAAAATAGCAACAAATTACACCAAACATGTCTTGTGCCTTATTGCGCCGCGTGTATAATAGAGGGCCCATGGTGCTTATAACATTTTTGTTAAAAAATATAAATATATTTTAAAATAGAAATTTATTGTAACTTTTTAAAAATATGTAATGTCTGTCATTTTGATGAATTTATGGTATCCTTGCTGACTTGTTTATTCTAGTCTTTAGAATAGTAATGTATAGTATATAGAATGGAGTCTATTGACATATATATATATATATATTTGTTGTTGTTGTTGTTGTTGTTGTTGTTGTTGCTGCTCTGGTATTTTCCACAAGCTTGTGTAAAACCTGATTGTCATATTCTCCAGCATAATTTAAAAATGATCCAAACAGCATACATCAGATGAAAACAATTTTTTTTTCTCCCTTCAGATCTTGTCAGTGCGTCCAGATGGC[C/T]AGGTAACACTTAAAGAGGGAGGTGGCCGCTGTGCGGTTGAGCTTCTCTTCTCTCCTCAGCAGCGCATGCCTCCCTTCACAGAGGAGCTGCAGTTGGAGTGTTTAGGTGCTGTTCGCCCCCTGCTGGTCATGAAGGGCTGCTGCCAGGCAGTGGAGGTCCGGCTGGACATTGACTACCTACAGTTTGGAGCTGTGGTCCAGCGATGCCAAGCCACTCGTCGTATTATCATGCACAACTCAGGAGACATTGGTGCGAGGTACATGTTTATGCATAAAATGCTTGATGGAATAGCTTAGAATTAGCCACACAGCAGCTAGAGCTTGAATTAATCAAATCTGTTATGAATAGAAAAGATAATAATATAAAATCTGAATCTACTATAATAAATCTTAAAGGTGTTTGGTCAATCTTTCAGATGCTTCTGTTAATAATTACATCTCTTTGTAAGCATTTTATCTTGGCTTCAGTGTTGGCTTTCAGCTTACAATCTGAACAGGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44889
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Essential Splice Site | 4316 | 4812 | None | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1145 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21174818)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21405041 |
GRCz11 | 18 | 21394107 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACTCACTCTCACTGGCTCCTGCATTGTCCCACCAGTCGCACCAGAGG[T/C]AATAGACTGAAGAAAACACTGAATGCAACAGTGTCACTTTCCTTCACTAA
Long Flanking Sequence:
GCACTCTCCAAAAATGTACTGTATATAGCGGTACGTTTTCAGGATGAGCCTGGGTTGATATTTTTATTCAAACAAATGCAGCTTCATAGCTTCTTTTAAAACAACAAACAAACCTTACTGATCCCAAACTTCTGACTCCACTGAATAATTAGGAATTTTTCAAATTTGGTGACTGGTTGCATACTAAAATGTACAGTTAGTTCTGTAAATTAGTCTAAATGACAATACTATACCATGTCAAATGTATAGTACAAATGAACTTTTCCACATTCTTCTCAGATTCAAATGGGATGTAAAGAGTTTTGCTCCAGATTTCACCATTTCACCAGCTGAAGGCTACATCACCCCAGGGATGGAAGTTTCACTTGAAGTGACCTTTGCGCCTACAGAGCTAAGACAAGACCTCCGTTATGATGATCTCTGCTGTTCAGTAGAAGGGGGAAAATCTTTAAAACTCACTCTCACTGGCTCCTGCATTGTCCCACCAGTCGCACCAGAGG[T/C]AATAGACTGAAGAAAACACTGAATGCAACAGTGTCACTTTCCTTCACTAAGTATTTGAATGTTGCAAATTTACTTAGAAAAATGTTGAGAAGTTAAAAGGCTGGACTGTTCATCATGTTACTGTCTATTTCTTGCTTTTTTTCTCTTTTGTACGAGCAGGTGGTGAATTTCGCATGTCAGGTGCGCAGTCAGTGCACACAGTCTCTGGCTTTGCCCATCCGCATTAACCAGCAGTGGACTCTGAAATGTGTCATAGAGGGAGAGCACTGGAGCGGGCCACCCACTCTCCTCACTGAGCCTACTCAACAGAACACCTATGAGATCACATACAAGCCGCTGGTCATGACTACTGATGGGGAGAAGCATGAGGTGTGACACTGTCTAGACAAGATGAGGGATCTTCAAGTCATTATTTTTTATTTTTGGAGAAGCTATTAAAGTGAAAAACAAATGTCACAATTGTCAATATAAAAACCCCACAGCAATTGTCAATGGCAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23295
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079297 | Nonsense | 4369 | 4812 | 76 | 81 |
ENSDART00000100830 | None | None | 140 | None | 4 |
ENSDART00000136934 | None | None | 582 | None | 11 |
ENSDART00000139351 | None | None | 268 | None | 4 |
ENSDART00000142807 | None | None | 161 | None | 2 |
ENSDART00000143265 | None | None | 1388 | None | 24 |
ENSDART00000147321 | None | None | 1146 | None | 21 |
Genomic Location (Zv9):
Chromosome 18 (position 21175136)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21405359 |
GRCz11 | 18 | 21394425 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGCGGGCCACCCACTCTCCTCACTGAGCCTACTCAACAGAACACCTA[T/A]GAGATCACATACAAGCCGCTGGTCATGACTACTGATGGGGAGAAGCATGA
Long Flanking Sequence:
CATTTCACCAGCTGAAGGCTACATCACCCCAGGGATGGAAGTTTCACTTGAAGTGACCTTTGCGCCTACAGAGCTAAGACAAGACCTCCGTTATGATGATCTCTGCTGTTCAGTAGAAGGGGGAAAATCTTTAAAACTCACTCTCACTGGCTCCTGCATTGTCCCACCAGTCGCACCAGAGGTAATAGACTGAAGAAAACACTGAATGCAACAGTGTCACTTTCCTTCACTAAGTATTTGAATGTTGCAAATTTACTTAGAAAAATGTTGAGAAGTTAAAAGGCTGGACTGTTCATCATGTTACTGTCTATTTCTTGCTTTTTTTCTCTTTTGTACGAGCAGGTGGTGAATTTCGCATGTCAGGTGCGCAGTCAGTGCACACAGTCTCTGGCTTTGCCCATCCGCATTAACCAGCAGTGGACTCTGAAATGTGTCATAGAGGGAGAGCACTGGAGCGGGCCACCCACTCTCCTCACTGAGCCTACTCAACAGAACACCTA[T/A]GAGATCACATACAAGCCGCTGGTCATGACTACTGATGGGGAGAAGCATGAGGTGTGACACTGTCTAGACAAGATGAGGGATCTTCAAGTCATTATTTTTTATTTTTGGAGAAGCTATTAAAGTGAAAAACAAATGTCACAATTGTCAATATAAAAACCCCACAGCAATTGTCAATGGCAGTGTATGCCTAATGCTGCGACAAATTTAGATATTTTTAATGACTTTATACCCCTCTGCTGTGTTATTAGCGTGTTGCTAGCATTTTTAAAACATTGCTAGTGTTGTCTTTACTTGAATTAAATTGTTTTGATATCTTTCAACCATAAATTACCATGCTGATAGCATGTTAAAGTGTATTGCTAGCGTAATTTATTTATCAAATCATGTGAATTGATACTTTTCCTCTGGGTGCTCCAGTTTTCCCCTAAAACAGTAAATTGGCCATAGTGTGTGAGTGTTTATGAACTCTCAGGGTTCAGTACTTGGGTTAGTGCACCTCA
Associated Phenotype:
Not determined