ZMP
si:ch211-152b13.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B0R0L6]
Human Orthologue:
C2CD3
Human Description:
C2 calcium-dependent domain containing 3 [Source:HGNC Symbol;Acc:24564]
Mouse Orthologue:
C2cd3
Mouse Description:
C2 calcium-dependent domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:2142166]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11196 | Nonsense | Available for shipment | Available now |
sa35824 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35825 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa28416 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22599 | Nonsense | Available for shipment | Available now |
sa35826 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32023 | Essential Splice Site | Available for shipment | Available now |
sa42505 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1436 | Nonsense | Available for shipment | Available now |
sa13118 | Nonsense | Available for shipment | Available now |
sa35827 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11196
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 |
---|---|---|---|---|---|
ENSDART00000112974 | Nonsense | 95 | 2194 | 2 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 14280313)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15325276 |
GRCz11 | 15 | 15261298 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGACACGCTGAACAGAAGGGGCTCAAATCCACAGCTCGCTTTCCTGTT[C/T]GATGTGGACCAAAACAGCTGACTTCTTATTTAACAGGTCTGATTGTTTGT
Long Flanking Sequence:
AGTGAAAAAAGACAGAGCCACACAGTTTTTTGACCTGAGTTTATTGTTATACTGCATGAGAATTTAGTAAAAAAACGTTAATTGGAACAAAACCATGTTTAATTTTCATAACCATAGCTTTTTATAGCAAATCTGTGATTCTACAATTGTATTACTATGGTAACAACACATTTACCCTAATAAAACCATAGTTATTCTTTATAAGTGTTCACTTTTACCATCCACTTTCAACTTTTTATTATGATCGTATTTGTTCTCCGCTCTCTGCAGTGCTCAGCGACGTGTCTCCGTCCACCAGCATTCCTCCTCTGGTTGAAGGCCAGCTAAGATGCTTTCTGAGAGTGACGGTCAGTAAAGCGCTGTGGACCATCATCAGACCTCCACCTGTGACTCTGATCAGACTTAGATGGTGGGGAGAGTCTTCAAACGGCACTTTCTTTAGGCCTAGAGATGGACACGCTGAACAGAAGGGGCTCAAATCCACAGCTCGCTTTCCTGTT[C/T]GATGTGGACCAAAACAGCTGACTTCTTATTTAACAGGTCTGATTGTTTGTGAATCTATTATCTAACTTTATATAAGGCAGTGTGTGTGTAGCTTAGTTTTTGATTATGATGTAAATGTGTGTTTTTCGTTTGCAGATATGGGCTCGCTGGTGCTAGATGTGCTTACAAAGGTTGATCATTTGCCTATAGCTCAAGCTCAGATTCCAGGAATCGCCCGGCTGTCTTTTTCACACTCCATAAACGGATATTTCACTCTTGTTTCCCCGACATCAGAAAAACTCGGAGAGCTTCAGGTGAATGAGATGCTGCTGAACGATTTGTTGTGTTGTAACATACTGTAGGTTAGGGCTGCATGATATTGGAAAAAAACTGATATTGCGATGTTTAGTTTTTCTGCAATATATATTGCAACATGAACAGAATTTAAACAGACAACTTGAATAGGTTAGTTTTGAAAGACTTCATTTTATATTGATTGGGTGGATTTTGTGAGACAGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35824
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 |
---|---|---|---|---|---|
ENSDART00000112974 | Essential Splice Site | 222 | 2194 | 4 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 14282355)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15327318 |
GRCz11 | 15 | 15263340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGCGTGTGAAGGAGACAGATGCCAGCAGCTCTGGACACATGCCCAGG[T/C]TTGATCATTTGACTGCTGAATGAACAAAATCTAATTGAATCACTCAACTG
Long Flanking Sequence:
TGATTATATAATGCTTTACATGTATTGTTTATTTTTAGTTTATGTAAATGCATTAATCAATTGAACTTTATTGTAAAGTTTGAGCTTTATTATTTATTTATAATAATAATAAAATTAATGTAACAAAATAAAATTATGTAATTATATAAATAAAATAAAAATAAAAATTTTTTATTTTTTATATAATTTTTTTAAATTTCTGTTTTCATTTTTTATTTCAGTAATTATAGAATTTTAGCTCATTTTATTTCATCACGTTTTATGTTCTACTGTATGTTGAATTATACATTAGCTTTTCTCATATATTATAGGTCACACTTGCCCTGGAAGCGTTAACAGAAGGATATGAGAGCAGTAGTTCAGTGCCCACTACTGATATGAGCCTCGACGCACAGACTCTTGTTGTAACCGACCACAACAAGCCAGTCCGGCCGTCCCTGGATCAGGCTCTGTTGCGTGTGAAGGAGACAGATGCCAGCAGCTCTGGACACATGCCCAGG[T/C]TTGATCATTTGACTGCTGAATGAACAAAATCTAATTGAATCACTCAACTGACATGCTTATAGGGCATAGGGCTTTTACAGCTTGGCTCAGATTTTTACCCAAATATTTTTATTAACATCACTTTTTTTTTTTAGTTTTAACATAGACACACATACACAAACAATACAGAAATAACACAAAAAAAACTTAATAAATAAAAAGAGAATGGAACCAGCAGGTCACCAGAGATGTCATTAAAGACAAACAAGATAAACTTTCAGAAAACAGCCCGGAAACATTATAATGCGCGCGCTCGTTAATATAAACCACGGTTGTCTTCAACTGTTGTCTTCAACGGTCTCTTTGCTCAACAACTCTGCTGAAAAACAAAGCAAAACATTACAACAGTCAGACATAGAGCAAAGAGCATAGAATCACCAAGAGGCGACTCTCTTTAATCAGGTCTTGATTTTCCTTGTTCATGCCACTCAACCTAGTCGACACACATCGAGTCACCAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35825
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 |
---|---|---|---|---|---|
ENSDART00000112974 | Nonsense | 403 | 2194 | 9 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 14285283)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15330246 |
GRCz11 | 15 | 15266268 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGTATAGCTGTAATATGTTTTCTTATTTTAGATGTCAGATGAATGTT[T/A]GGAGGAGGACCATCATAGAAAAGGCACAACAGAGAAGCCTGTGCACACAA
Long Flanking Sequence:
TGTTTCCCAGAGCTTGGTAGTGGCTGGAAGGGCATCCGCTGCTTAAAGACGTGCTGGATAAGTTGGCGGTTCATTCCGCTGTTGCGACCCTGGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAAAAAGGGGCATAATATGTCTCCTTTAAGTGAAGAAAATGAAACTTTGCTTACAAATATTTAACATAGTTGTTTGAATCTTTTAGAGTGAGCTTGACGTTTTGGTCTGTGGATCTTTTCATCAGTGTTAATGGATCTGTGCTGCAGTTCTGGGACGGCGAGGGCTCTCTTGCAGATTCTCTGTCTGATCACAGCAGTGTGCTAATGGACAGTGAGCTCAATGACCCTCAGTATGATCAGAGTCTTCTGGAGAACCTCTTCTACAAACCACCTGTAAGCCATGCAATGCAACCCAATGAACTAGTTCTGCAAACATTGCTGTGTATAGCTGTAATATGTTTTCTTATTTTAGATGTCAGATGAATGTT[T/A]GGAGGAGGACCATCATAGAAAAGGCACAACAGAGAAGCCTGTGCACACAAATCCAGCCAAAAATGCCCGGTCAGTTAGTGTAATACAAGAAACAAGCCCCAAAACTCAATTGATTGATTCATTTTTAGTGTAATTTAATAAGAACTTATAATAACATTTAATAATTTCAAATAATCCTGATTTTCAGAAACAGATTTATGCATTGTACTTTTAATTTAGGATATATTATAACATTGTTTCTCAACCACGTTCCTGGAGGACCACCAACACTGCATATTTTGGATGACTCCTTTGTCTGTCACACCCATCACAGGTCTTTCAGTTTCTGCTAACGAGCTGAAGATCTGAATCAAGTGTGTTTGTTTAGGAGACATGGAAAATGTGCAGAGATGGTGGTTCTTCAGGAACGTGGTTGAGAAACAATGTAATATAAAATAATATATTTAATTATATGCTGAATTGATAAATAAAAAAAAATATGCACAAAATGTAAAACATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28416
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 |
---|---|---|---|---|---|
ENSDART00000112974 | Nonsense | 492 | 2194 | 11 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 14286564)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15331527 |
GRCz11 | 15 | 15267549 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTATTAAAACTAACCTAATGCACACTTGTCCTGTTTGTCTAGTTTTTA[T/A]ATTGTAGAGTACCTCTTTCCACTGCTCTCTGCTGGGTATGAGAGTGTTCA
Long Flanking Sequence:
GATTCATAAAGGTACACAAATATTTGTACAAGCATTAACAAATATAATTATTAAATAAATAAAAATAAATAAATAAAACAATATTACTAACACAATGAAATAAAATGTATTTAAGTAAAATAGGATAAAATATATTTCAAATACTTTTTGTTTTTAACTTTTATTCCTGTTCTTTGTGGTGAAAATTCTCTCTCCTTTTTGAAGGCTTGATCCTGGTGTGCAACATTCAGAAGCAGGAGCTGATTTACCTGGGCTTGGCATGGAAAAAATAACTTTGCTTGGTGATATTCGTTTTGCGAGGGTCACTGTCAGTGAGTTAAAACTTCCTACAGAAAGTACCTCAAAAAGTCTGTCTAGAAAAGGAAGACCACCTCGGCCTCTCTCCACAAAGAAGTGGTATGACATTTAGGATAAATCAGAAAAGATGACGGTCACTAGAAATCAGTTTCAGTGTATTAAAACTAACCTAATGCACACTTGTCCTGTTTGTCTAGTTTTTA[T/A]ATTGTAGAGTACCTCTTTCCACTGCTCTCTGCTGGGTATGAGAGTGTTCAGCAGGTTCCTTCAGAGATTACAAAAGTTGTCTCTAGTAAAGTTACAGATGGTGGTGAGTACATTAGTTTTGAAGAACTTTAATAAAACTTAAGCTGACAACAATCTGCTATTTATTTATTTATTTATTTATTTATTCATTCATTTTGCTTTAGCTGTGTCGTTTCAGCATCAAAGTTTGTTTCCAGTGAAGTTCAGTAGGTCATCTATTAAACAGTGGTGCGAGATGAAGGTCACATTCAAGATCTACTCCAAATATAGTCTTCAAAAAACAGTAAGTGCAACGTGTCAATCATAAAATCTACACACTTCAGACTAAGCTGAAAACTAAAGACTCTTGTATGATTTTATCTGGCCTGATCTTGCCTTGTTTGTTGTTTAGCCTATTCTGATTGGCTCAGCTATGTTTCCACTGAGCTCCTTGATGCAGAGTGAATCGCTGAGCATTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22599
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 |
---|---|---|---|---|---|
ENSDART00000112974 | Nonsense | 824 | 2194 | 16 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 14291284)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15336247 |
GRCz11 | 15 | 15272269 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGGAGCTGCTCCTGCAGTCTCAGTATCCAGTGGTTGGAGTGGACAGTTA[T/A]ATGCCTGTGGTGGATGTATTTAGCGGCAGCACGCGAGGAAACCTCAGGGT
Long Flanking Sequence:
ATTCACATATTGTGATATTGATGTGAAAATGAGATATTGTGAAGCCATAATGTGTGTAAATATACATATACAATGCCCAGAATAAATGTTTCAAGCTGATTCTAAATATAAGTATATTAGTCAAACTGAAATAACAACAGGTGGCACGGTGGCTCAGTGGTTAGTGGTGTCTCTGGTTTAAGTCTCAGTTGGACCAATTGCCATTTCTGTGTAGAGTTTTTGCGTCAGTTTCCTCTGGGTGCTACGGTTTCCCCCACTTTCCAGAGACATTCGTTATAGGTGAAATGAGTAAGCTAAATTGGCCGTAGTGTGTTGGCGGTTCATTCAGCTGTGGCAACCCCTGATGACTAGGGGACTAAGCCGAAGGAAAATGAATGAATTACTGAATGAAATAACAACAGAACATAGATCTGTAATTAACCTTTTTTTCTTTTCAGAGACCCCAAGATCTCGGAGCTGCTCCTGCAGTCTCAGTATCCAGTGGTTGGAGTGGACAGTTA[T/A]ATGCCTGTGGTGGATGTATTTAGCGGCAGCACGCGAGGAAACCTCAGGGTGTGTTTAGCAATGGGTCAAGCACAGCAGGTCATGGCCCTGCAGCGGATGAGGGACGACGAGCTGAGCCACGACACACCAGTGCCTCGACCAGCACACATGCTAGACCACCGGCCACACACGGAAGCCAAGGCAAGTTTACGCTGCGATAGAATGCATGTACTTTAAGATATTTATATGAATATTTTAACATTTTAGATTTAAATAGGTTTTATATGCTCGTTTATAACTGCAGGAATTACATATATAATAAAAAGCTTGGTTTTATAATAGTCATAAATATCAATGAGCTCGTCTAAGACTCTCCGCAGCTCATGTCATTACCTGACGTTGACACGTACACACACACACAAACTCACACTCACATAGTGTGACATACTCTGAAATACACATACAAAATTACCATACTTCAGTTCTCCTAAAATATTGACTAGATACCTTGTTAAATGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35826
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 |
---|---|---|---|---|---|
ENSDART00000112974 | Essential Splice Site | 941 | 2194 | 17 | 35 |
ENSDART00000112974 | Essential Splice Site | 941 | 2194 | 17 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 14293061)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15338024 |
GRCz11 | 15 | 15274046 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCCAGAATGAGTCAAGAGAGGACATGGACACACATGCTGTCGAGAGCC[G/T]TAAGCTGGTTCCTTGCTCACTGTATATATATAACCTTTGATTGAGTTTAA
Long Flanking Sequence:
ATGCACCAATGACCATGGCAGTCTCCATAGACTCCTGACATCTAAGCCACTGATGACATGGAAAATAATCCTTTTGGCTTTTTGTCTGTGTGAGATTTGATTGTTTTGTCGTTTCTGGAGTGTCAGAACAGTGGTTAAAGCTCCGCCCTCTTCTGGAAAGCAGCAGCTCATTTGCATTTAAAGACACAGACTTAAAAATTGATCGTTGGTGTATTTTGAACTGGAACTGCACAGACACGTTATGGGGCCACCATATATTTATTTGACAACTTAAAAACAATGTCCCATATTAAAATGGACCCTTAATGTATGATGAATATTGTTTTAGGCCACTTCAGATGTCCTGCTTGAGCATGTGTTCATGGTCCGGGTCGAGAGAGTAAAGGGTCTGATGCCTCTGCAGTCCACAGTATGGGGTGAAGCCGACTGCTATATCCAGTACTCTTTTCCTGCCCAGAATGAGTCAAGAGAGGACATGGACACACATGCTGTCGAGAGCC[G/T]TAAGCTGGTTCCTTGCTCACTGTATATATATAACCTTTGATTGAGTTTAACCAGCTGTATTTTGCACAGACGTGGACTTGAAAGCGTTCCGCTCTGAGACCACTCTCTGTGTGCCCGACCCTGTGTTTGGACACAATGAGACTCACGTCCTGCTGGCTCCGCCTGACGTCCCAGTGCAAAAGCTACTGCTAAACTCACTGGCCCATCAGGGACTGAGGGGTGGAGGAGGAGTGCAGTTTGAAGTTTGGTGCAGGTACTGTTTGATGTTTGTTTATTTATTCTTTTATTCATTCATTTATGATAACGTGGATCCCTAATTTTGAAAAAATATATTATTTTATTTATTTGTTTGTTTACATTTTAGCATTTCAAGGAAGAGCCTCTTTTGTTTGATAATATTTCAATTTTAGTTGTATTAAATAAAAAAATAAAATGCATTTGGTTTTAATATTTCTTGTATTGATTTTCAAGTATACACATTCACAAACCACACAACTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32023
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 |
---|---|---|---|---|---|
ENSDART00000112974 | Essential Splice Site | 941 | 2194 | 17 | 35 |
ENSDART00000112974 | Essential Splice Site | 941 | 2194 | 17 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 14293061)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15338024 |
GRCz11 | 15 | 15274046 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCCAGAATGAGTCAAGAGAGGACATGGACACACATGCTGTCGAGAGCC[G/T]TAAGCTGGTTCCTTGCTCACTGTATATATATAACCTTTGATTGAGTTTAA
Long Flanking Sequence:
ATGCACCAATGACCATGGCAGTCTCCATAGACTCCTGACATCTAAGCCACTGATGACATGGAAAATAATCCTTTTGGCTTTTTGTCTGTGTGAGATTTGATTGTTTTGTCGTTTCTGGAGTGTCAGAACAGTGGTTAAAGCTCCGCCCTCTTCTGGAAAGCAGCAGCTCATTTGCATTTAAAGACACAGACTTAAAAATTGATCGTTGGTGTATTTTGAACTGGAACTGCACAGACACGTTATGGGGCCACCATATATTTATTTGACAACTTAAAAACAATGTCCCATATTAAAATGGACCCTTAATGTATGATGAATATTGTTTTAGGCCACTTCAGATGTCCTGCTTGAGCATGTGTTCATGGTCCGGGTCGAGAGAGTAAAGGGTCTGATGCCTCTGCAGTCCACAGTATGGGGTGAAGCCGACTGCTATATCCAGTACTCTTTTCCTGCCCAGAATGAGTCAAGAGAGGACATGGACACACATGCTGTCGAGAGCC[G/A]TAAGCTGGTTCCTTGCTCACTGTATATATATAACCTTTGATTGAGTTTAACCAGCTGTATTTTGCACAGACGTGGACTTGAAAGCGTTCCGCTCTGAGACCACTCTCTGTGTGCCCGACCCTGTGTTTGGACACAATGAGACTCACGTCCTGCTGGCTCCGCCTGACGTCCCAGTGCAAAAGCTACTGCTAAACTCACTGGCCCATCAGGGACTGAGGGGTGGAGGAGGAGTGCAGTTTGAAGTTTGGTGCAGGTACTGTTTGATGTTTGTTTATTTATTCTTTTATTCATTCATTTATGATAACGTGGATCCCTAATTTTGAAAAAATATATTATTTTATTTATTTGTTTGTTTACATTTTAGCATTTCAAGGAAGAGCCTCTTTTGTTTGATAATATTTCAATTTTAGTTGTATTAAATAAAAAAATAAAATGCATTTGGTTTTAATATTTCTTGTATTGATTTTCAAGTATACACATTCACAAACCACACAACTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42505
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 |
---|---|---|---|---|---|
ENSDART00000112974 | Nonsense | 1534 | 2194 | 26 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 14306743)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15351706 |
GRCz11 | 15 | 15287728 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTGCTGACCTGCAGTATCTTGTGTTTGCTGTTTTGCATGTCAGGTTG[T/A]CCTCTGGCTGAAAGAGGGGGAGGGTTGCCAAGTTGTTGTGTTTCTTATGC
Long Flanking Sequence:
AATACAAGTTTCCTATTTAAAAACAAACTTTTTTTTGCTCCTGCATTAAATCACAAATCCTCACTTTAACAACACTTAAAGTACATGCATTAAACTTTACCGCATTATTTACATCATATCTATATTCTGAAGGTTTGTACAGAGAAATATGTTTATACATTGTTTGCCTGAAGATCTTTCTCGTAACATTTTCTGAATTATGGACTGATAATAAAGATCCCACTCCCAATCCCAAAAGAGATCTCCAAAATTGTATTACTCTAATATGTGACAAAATGAAACCAGTATTTTGAAACGGACCTAATTCAAGGTTCATTTTTTTTTGTGCTGGAAATTAATACAAATTAGTGCATATTTAATTGATGTATTTGCATATTTATACATGCATTTTAGGAAACTTATTTTTTAATGTACAGTAAGTTGTGGAAGTGTGATAATTAGGTAATCGTTTTATTGCTGACCTGCAGTATCTTGTGTTTGCTGTTTTGCATGTCAGGTTG[T/A]CCTCTGGCTGAAAGAGGGGGAGGGTTGCCAAGTTGTTGTGTTTCTTATGCCACTGCTGATGACACGGGTACAGTGACCACAGCGCTGATTAAAGACAATGAATGTCCTGTGTGGGACCACCAGCAGGAGTGCAGGTATACCCATTTGACACGACTACATATATATATATATATATATATATATATATATATATATGTAGTATATATGTAGTATAAACTAGCCACTTTGGCTGGTTGAAAATAATTTTTAAATTGTGGTTTTCTTAAAAGCAGGGTTCTACTATAAGAATGACCCATAATGTGTGCACATATATATATTTTATATCTTAGTATAAACAAGCATTTTTTCAAATATATGCATGCATTTGTGTATGTTTGTATGTTTGTATGTTTGTATGTTTGTATGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1436
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 |
---|---|---|---|---|---|
ENSDART00000112974 | Nonsense | 1658 | 2194 | 28 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 14308606)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15353569 |
GRCz11 | 15 | 15289591 |
KASP Assay ID:
554-1363.1 (used for ordering genotyping assays)
KASP Sequence:
AAGTGTCTGTGTCTCCTCTGAGAGCAGTGCAAGAGCTGCGGGCACATAGA[C/T]AGATGGCACAGGACACTCATGCTCCAGACTCCAGTGTAAGACATTATTTA
Long Flanking Sequence:
CATATATTTCTTTTTGATATTTTGATGCATTAAAAATGATTTGAATTACAAATCTTCAGAAATATTATAAATGTTTTTTATGCAAAAGTGATGGTGATATTTGTTGCAGTATAGACAACTGGTCATTTCTGCTTCTGAAAAATCAAGGACGTGTTCACAATAAACGTGTGTTTTATGTTTTCAGACTGTCAAAAGAGCTACTCTTGGATCCCCAGCAGTGCTTGGTTTTTAAAGTTTGGCATAAAGGAGGTAAAGACACACTGCAATTCTCCATGACACTGTGTTTGTGACAGTTTAAAAGATTACTGTGCAATGGTTTTCCCCTTGCAGAGGTGGAGCGGGTGATTGGGTTTGTGTCTGTTGACCTGTCACCTCTTCTGTCGGGATTCCAGTCAGTTTGCGGCTGGTACAACATCACTGATTTCAGCGGGCAGTGCCAGGGGCAGTTAAAAGTGTCTGTGTCTCCTCTGAGAGCAGTGCAAGAGCTGCGGGCACATAGA[C/T]AGATGGCACAGGACACTCATGCTCCAGACTCCAGTGTAAGACATTATTTATATTTATTATGTATTTATTTATGTATTTATTTAATAATATTTTTCCTACAGATTTATTATCATAGTTTGCTGTTTGGTCTACCAAGTGTTTTATCTGTGACTATTTGCAGTTGAAGATAGAAGAAGTGTCTTAGCATTATGTCAAATAACAGTGTATTCTATTTTTATCGTAGGTACAAGAGTAATTTAAAATTTGATAACTACTTGACAAGATTTTTATACTAAGAGCACTTTGTTGTGTTTTTATACGTGTATTCTAGTTTTTTTTCCATATAATGAGCTGAAAATCCTTTCTAATTATTTTATTTTATTCATTTATTCATTCATTTTTGGCTTATTCCCTTTATTAATCTGGGGTCGCAACAGCGGAATGAACCGCCAACTTATCCAGCGTTTGTTTTACGCAGTGTATGACATTCCAGCTGCAACCCACTAGAGGGAAACATACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13118
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 |
---|---|---|---|---|---|
ENSDART00000112974 | Nonsense | 1923 | 2194 | 32 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 14316986)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15361949 |
GRCz11 | 15 | 15297971 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAAGATGAAGAAAAAAACGATCACATCTCCAGTGATGATGATGAAGAT[A/T]AAGACCAGGATGAGCATGTAGACTTTGAGGAAACTTTAATTCAKCCYAGA
Long Flanking Sequence:
GTTTAATAAACCTGTTTTTAAAATGACCTAAACAGTATTGGCTACAGTATATTCAATGAGAGATGGATAAAACATGTTCATTAACAGAAGGGGGTGAAGTTGTTTATGCTGAGCACTATATGTGTAGTTTAGTTTGAAGTATATCAGGGATAGATAGTGATATCCTATTTATTTAGGTCATTTTTCTCATGATATTTTATCTTAAATCAGGTTTAAGTGAACATCAGCCTGAAGAAGCACCTGTTATCCTTAAAAGCACCACCACTACTCCTGATGTGGCTGATAAGCGTTTAACCTCTGGAGCTGATCAGCTGATTCTAACAGAGTCGTACAGCTGTGAGACAGAACCACACTTTCATAAACACTCTGACATGATGCTGGAGGATGAAAATGAAGTCTCGCCCTTCAGCTCTCCTGCTCCTACAGAGACCAGACACTCAGTAGCTGCTCCAGAAGATGAAGAAAAAAACGATCACATCTCCAGTGATGATGATGAAGAT[A/T]AAGACCAGGATGAGCATGTAGACTTTGAGGAAACTTTAATTCAGCCCAGAACATTAAATGAGGTCACTTCAGTCACAGACAGAACCAGCCCCTGGACCAGCTTGCTGTCTGACCCAGATATGAGCTCTCTAGAGAGTCTAGAGTCTGTGCACCGTCATTCTCAGGACCACAGCATCCACATTGGAGGAGAGCAGAGAAACAGAAGTGACAATAACCCACTAACTGCAGAATCCCAAGAGACTGATTCTGATTCAGATGTTTCAGAAAGATCTCCAACTGGTCAGGAGATGTTTAGGGGAGCTGGTGCTGTTGAAACAGAACAGCAGGTACAGCAGGCTTCTCCAGATGGTCTTGATGGAGATGATGCTCTTTCTAGTATCAGTGAGGCAGAGGATTGTGAGCTGAGCAACAGTGGGCCTGAAGAAGCGATTGAAAGGCCAATATCATCTCCCTCTGCAGAGTCTGCCTCAGAAGCAGATGACAAACATGATGAGAAGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35827
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 |
---|---|---|---|---|---|
ENSDART00000112974 | Nonsense | 2115 | 2194 | 33 | 35 |
Genomic Location (Zv9):
Chromosome 15 (position 14317778)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 15362741 |
GRCz11 | 15 | 15298763 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAAATTTCTTCCTGTCAACTCACCATCTGGAGGCGTCCATGAGGGCTT[T/A]GAGGATGGCGCCTGTTTTTCCAACAGCTGAGTCTGTGAGTAATCGAACTG
Long Flanking Sequence:
TTAGGGGAGCTGGTGCTGTTGAAACAGAACAGCAGGTACAGCAGGCTTCTCCAGATGGTCTTGATGGAGATGATGCTCTTTCTAGTATCAGTGAGGCAGAGGATTGTGAGCTGAGCAACAGTGGGCCTGAAGAAGCGATTGAAAGGCCAATATCATCTCCCTCTGCAGAGTCTGCCTCAGAAGCAGATGACAAACATGATGAGAAGACAACCAAAATGTATCCTTTGAAGCTTTGTGTGGATATTTTGGTTTTCTGTATTGTAGAAGTATTCAAATGAATTTAACAGCATATTATACACTGTAATATTGATGCCACCAATGAGCAGATGCTCTATTTTCAAAGGTGAATCTACTTGTATGATGGTGGTATGTTAAACCGCTGCAGGCATGAAGGGATAGTATGGTTGTGTTGTCCTGAACCCCTATTTGCAGTTTGGAATCTGTTGATATTCCAAATTTCTTCCTGTCAACTCACCATCTGGAGGCGTCCATGAGGGCTT[T/A]GAGGATGGCGCCTGTTTTTCCAACAGCTGAGTCTGTGAGTAATCGAACTGTTTGTCTGTCTAATCCACCGTTCAATCCATCATTCTGTAGCTATCGTGATTAGAGGGGCAACAATATAGAGTTCTCAAGATTCGGTTTGGTTTTCGGTTTTAGGGTCACTTTTTTGGTATTGTTTATGATATGTTATAATATGTTATAGATAGCACTGCCAAAAAAAAGTAAAGGGGAAAAAATCTTAGAGCTAAATACAATACAAATGAATATAGCAAAGATAATACTAATATAAACTGAAACAGGAAAAATATAATCAAATATAATATCTTCAATGTATAAATGAAATGTTTGCCATTATTGAGCTACAGTAGCCTTTATAGCTATTCGGTCAAGAGTGGAGTGAGTGATTTTGTTGTCGTTTGTTGTTTAAATTCTATTAAAAGCACGGAGAGCAGGGATAAAATGTTTTTCATTCAAAATGCTGTGGAGATGTAGCACAATGTGGA
Associated Phenotype:
Not determined