Busch Lab

ZMP

si:ch211-245p7.3

Ensembl ID:
ENSDARG00000056764
ZFIN ID:
ZDB-GENE-050419-219
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
sa17962 Nonsense Available for shipment Available now
sa10786 Essential Splice Site Available for shipment Available now
sa12926 Nonsense Available for shipment Available now
sa12486 Essential Splice Site Available for shipment Available now
sa36645 Essential Splice Site Available for shipment Available now
sa17202 Nonsense Available for shipment Available now
sa16299 Splice Site, Nonsense Available for shipment Available now
sa12927 Nonsense Available for shipment Available now
sa14679 Nonsense Available for shipment Available now
sa32205 Nonsense Available for shipment Available now
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.
Availability:
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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:
sa17962
Status:
Available for shipment
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Availability:
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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
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Availability:
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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:
sa12926
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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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:
sa12486
Status:
Available for shipment
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Availability:
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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:
sa36645
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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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:
sa17202
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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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:
sa16299
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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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.
Availability:
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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.
Availability:
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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:
sa32205
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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:
sa23295
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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