ZMP
vmhc
Ensembl ID:
ZFIN ID:
Description:
ventricular myosin heavy chain [Source:RefSeq peptide;Acc:NP_001106204]
Human Orthologues:
MYH6, MYH7
Human Descriptions:
myosin, heavy chain 6, cardiac muscle, alpha [Source:HGNC Symbol;Acc:7576]
myosin, heavy chain 7, cardiac muscle, beta [Source:HGNC Symbol;Acc:7577]
myosin, heavy chain 7, cardiac muscle, beta [Source:HGNC Symbol;Acc:7577]
Mouse Orthologues:
Myh6, Myh7
Mouse Descriptions:
myosin, heavy polypeptide 6, cardiac muscle, alpha Gene [Source:MGI Symbol;Acc:MGI:97255]
myosin, heavy polypeptide 7, cardiac muscle, beta Gene [Source:MGI Symbol;Acc:MGI:2155600]
myosin, heavy polypeptide 7, cardiac muscle, beta Gene [Source:MGI Symbol;Acc:MGI:2155600]
Alleles
There are 22 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32911 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18727 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10407 | Nonsense | Available for shipment | Available now |
sa19750 | Essential Splice Site | Available for shipment | Available now |
sa19751 | Nonsense | Available for shipment | Available now |
sa11779 | Nonsense | Available for shipment | Available now |
sa7497 | Missense | Mutation detected in F1 DNA | Not yet available |
sa18019 | Nonsense | Available for shipment | Available now |
sa15964 | Nonsense | Available for shipment | Available now |
sa25806 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25807 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19752 | Nonsense | Available for shipment | Available now |
sa19753 | Splice Site, Nonsense | Available for shipment | Available now |
sa5139 | Splice Site, Nonsense | F2 line generated | Not yet available |
sa32912 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32913 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5718 | Nonsense | F2 line generated | Not yet available |
sa2053 | Nonsense | F2 line generated | Not yet available |
sa18728 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10912 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32911
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099532 | Essential Splice Site | None | 1938 | 2 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23594437)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24614058 |
GRCz11 | 2 | 24269709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGCATCAATTGATTTTTAGTGACAGATAATTATTATTATTTTTTTAAC[A/C]GGTTCTTCTGCCTCCGCACTTGGTGCACATCAGGTATAAATCACACTTAT
Long Flanking Sequence:
GGCTTTTATCATTCACGTTTCATTTAAGTACAAACCACTTATCTCTTCCCCCTGTCTCTGAACTAAATTAGCCCTCCGCTATCAGAGAACCTAAAATGGAGAGCTAACAAATCTCTACAAAGATAAGACTTAACTCAACTAGCAGGTTCTTGTTTCTCGCTAATACCCCTAACTACATTTGCTGCACCTTAATAGTGGTCAGACGCAATAGGCAATAGCATTCCGGCCTTCTGGGATGCCTTCCCCAAATTTGGGAGGGTGACTTCCTTTATAAAGTGATCTCATGGTTGGTGTTCAGACAAGTCGGACGTTTCATCTGAGGGTAAGATTTGAGCAAAACTGCATGGTGAAGTTAGATTTAAGAGTAAAGGATTTTTTTTTTTTTTTTTTTTTTTTGCTGAAATGTCATAAATGACTTTTAAAAAACTTTTGCTTTGTTTATTTCTTTAAATAGCATCAATTGATTTTTAGTGACAGATAATTATTATTATTTTTTTAAC[A/C]GGTTCTTCTGCCTCCGCACTTGGTGCACATCAGGTATAAATCACACTTATTTTTTGTATTTAGGAATTAAGCCATAGTTATATTTTAAAGCTGGTTTTTATGCAATTGTGGGCAATACTTGCAAGTTTTAACTCACTTAACCAACTTCATCATCTCCAGACAAGGCAATCATGGGGGACGCTCAGATGGCAGAGTTTGGAGCAGCAGCTTCTTACCTGCGAAAGTCAGATCGAGAGCGTCTGGAAGCACAAACCCGTCCCTTTGATATGAAAAAGGAGTGTTTTGTGCCTGATCCAGATGAAGAGTATGTAAAAGCTTCAATCGTCAGTCGTGAAGGTGACAAAGTCACTGTACAGACTGAGAAAAGAAAGGTAGGCTTGACTAATTAATCATTTTGCCGCTTTAAAGGGTTGGAAATTTTAATTACACCTTTTAAAATTGGTCACTGAAACATTATGAGCACTATGAGGAATTTGTGCATAAGTGCATTAGGTCTTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18727
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 27 | 1938 | 3 | 39 |
ENSDART00000099532 | Nonsense | 27 | 1938 | 3 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23594686)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24613809 |
GRCz11 | 2 | 24269460 |
KASP Assay ID:
2259-1970.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCAGCAGCTTCTTACCTGCGAAAGTCAGATCGAGAGCGTCTGGAAGCA[C/T]AAACCCGTCCCTTTGATATGAAAAAGGAGTGTTTTGTGCCTGATCCAGAT
Long Flanking Sequence:
TTTGGGAGGGTGACTTCCTTTATAAAGTGATCTCATGGTTGGTGTTCAGACAAGTCGGACGTTTCATCTGAGGGTAAGATTTGAGCAAAACTGCATGGTGAAGTTAGATTTAAGAGTAAAGGATTTTTTTTTTTTTTTTTTTTTTTTGCTGAAATGTCATAAATGACTTTTAAAAAACTTTTGCTTTGTTTATTTCTTTAAATAGCATCAATTGATTTTTAGTGACAGATAATTATTATTATTTTTTTAACAGGTTCTTCTGCCTCCGCACTTGGTGCACATCAGGTATAAATCACACTTATTTTTTGTATTTAGGAATTAAGCCATAGTTATATTTTAAAGCTGGTTTTTATGCAATTGTGGGCAATACTTGCAAGTTTTAACTCACTTAACCAACTTCATCATCTCCAGACAAGGCAATCATGGGGGACGCTCAGATGGCAGAGTTTGGAGCAGCAGCTTCTTACCTGCGAAAGTCAGATCGAGAGCGTCTGGAAGCA[C/T]AAACCCGTCCCTTTGATATGAAAAAGGAGTGTTTTGTGCCTGATCCAGATGAAGAGTATGTAAAAGCTTCAATCGTCAGTCGTGAAGGTGACAAAGTCACTGTACAGACTGAGAAAAGAAAGGTAGGCTTGACTAATTAATCATTTTGCCGCTTTAAAGGGTTGGAAATTTTAATTACACCTTTTAAAATTGGTCACTGAAACATTATGAGCACTATGAGGAATTTGTGCATAAGTGCATTAGGTCTTTAGTATTAAAATGTTATTCATTTGTTGTCCTTCGGCTTAGTCTCTTATTTATCAGCGGTCACCACAGCGGAATGAACTGCAAACTTATTCAGCACAGGTTTTATGCAGCAGATGCCCTTCCAACTGCAACCCAGTACTGGAAAACACTCATACACACTTATTCACACATCTACACTACGGGCAATTTATCTTATTCAGTTCACCTATACTGCATGTCTTTGAACTGTGAGGGAAACCGGAGCACACAAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10407
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 27 | 1938 | 3 | 39 |
ENSDART00000099532 | Nonsense | 27 | 1938 | 3 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23594686)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24613809 |
GRCz11 | 2 | 24269460 |
KASP Assay ID:
2259-1970.1 (used for ordering genotyping assays)
KASP Sequence:
GAGCAGCAGCTTCTTACCTGCGAAAGTCAGATCGAGAGCGTCTGGAAGCA[C/T]AAACCCGTCCCTTTGATATGAAAAAGGAGTGTTTTGTGCCTGAWCCAGAT
Long Flanking Sequence:
TTTGGGAGGGTGACTTCCTTTATAAAGTGATCTCATGGTTGGTGTTCAGACAAGTCGGACGTTTCATCTGAGGGTAAGATTTGAGCAAAACTGCATGGTGAAGTTAGATTTAAGAGTAAAGGATTTTTTTTTTTTTTTTTTTTTTTTGCTGAAATGTCATAAATGACTTTTAAAAAACTTTTGCTTTGTTTATTTCTTTAAATAGCATCAATTGATTTTTAGTGACAGATAATTATTATTATTTTTTTAACAGGTTCTTCTGCCTCCGCACTTGGTGCACATCAGGTATAAATCACACTTATTTTTTGTATTTAGGAATTAAGCCATAGTTATATTTTAAAGCTGGTTTTTATGCAATTGTGGGCAATACTTGCAAGTTTTAACTCACTTAACCAACTTCATCATCTCCAGACAAGGCAATCATGGGGGACGCTCAGATGGCAGAGTTTGGAGCAGCAGCTTCTTACCTGCGAAAGTCAGATCGAGAGCGTCTGGAAGCA[C/T]AAACCCGTCCCTTTGATATGAAAAAGGAGTGTTTTGTGCCTGATCCAGATGAAGAGTATGTAAAAGCTTCAATCGTCAGTCGTGAAGGTGACAAAGTCACTGTACAGACTGAGAAAAGAAAGGTAGGCTTGACTAATTAATCATTTTGCCGCTTTAAAGGGTTGGAAATTTTAATTACACCTTTTAAAATTGGTCACTGAAACATTATGAGCACTATGAGGAATTTGTGCATAAGTGCATTAGGTCTTTAGTATTAAAATGTTATTCATTTGTTGTCCTTCGGCTTAGTCTCTTATTTATCAGCGGTCACCACAGCGGAATGAACTGCAAACTTATTCAGCACAGGTTTTATGCAGCAGATGCCCTTCCAACTGCAACCCAGTACTGGAAAACACTCATACACACTTATTCACACATCTACACTACGGGCAATTTATCTTATTCAGTTCACCTATACTGCATGTCTTTGAACTGTGAGGGAAACCGGAGCACACAAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19750
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099532 | Essential Splice Site | 68 | 1938 | 4 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23595407)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24613088 |
GRCz11 | 2 | 24268739 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACTTTAAAGTGTTATTTTAATAATTACAATCTTTCTGTTTTTCTCCC[A/T]GACTGTAACTGTAAAGGAAGCTGACATTCACCCCCAGAACCCTCCAAAGT
Long Flanking Sequence:
GAATTTGTGCATAAGTGCATTAGGTCTTTAGTATTAAAATGTTATTCATTTGTTGTCCTTCGGCTTAGTCTCTTATTTATCAGCGGTCACCACAGCGGAATGAACTGCAAACTTATTCAGCACAGGTTTTATGCAGCAGATGCCCTTCCAACTGCAACCCAGTACTGGAAAACACTCATACACACTTATTCACACATCTACACTACGGGCAATTTATCTTATTCAGTTCACCTATACTGCATGTCTTTGAACTGTGAGGGAAACCGGAGCACACAAACACGGGGAGAACAAACAAACTAACTCAGCCGGGACTCAAACCAGTGACCTTTTTGCTGTGAGGCGACAGTGCTAACCACTGAGCCATAGCGCCGCCATTAAAATGTTAGCTTCTGTATAATTTGTTTTGGAATTCTTTTAAAATATTGTGCACAATAACTCATTTGATGCCACTTTACTTTAAAGTGTTATTTTAATAATTACAATCTTTCTGTTTTTCTCCC[A/T]GACTGTAACTGTAAAGGAAGCTGACATTCACCCCCAGAACCCTCCAAAGTTTGATAAAATTGAAGACATGGCAATGTTCACCTTCCTTCATGAGCCAGCCGTGCTGTTCAACCTCAAAGAGCGCTATGCAGCATGGATGATCTATGTAAGAGGAGAATGATTCGTTGTCCCTTGAAAATCGCATCCCAATTAGCTTCAATTACTGAACTGCATTTGTCCTTTCCCACAGACCTACTCAGGACTGTTTTGTGTCACTGTCAACCCCTACAAGTGGCTGCCGGTGTACAATCAGGAGGTGGTTGTAGCCTATAGAGGGAAAAAGAGGAGTGAAGCTCCTCCCCACATCTTTTCCATCTCTGATAACGCCTATCAGTACATGCTAACAGGTACGAAACAAATCCTCAAATCTGTTCTGCTTAGCAAATTCGAGAGCACCTCTCTTTTACCTGAAAGCATTAATCAAATCAGGCAATATATCTCATAAAGGGTAAAAAAAAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19751
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 145 | 1938 | 5 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23595724)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24612771 |
GRCz11 | 2 | 24268422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGTGGCTGCCGGTGTACAATCAGGAGGTGGTTGTAGCCTATAGAGGG[A/T]AAAAGAGGAGTGAAGCTCCTCCCCACATCTTTTCCATCTCTGATAACGCC
Long Flanking Sequence:
CCAGTGACCTTTTTGCTGTGAGGCGACAGTGCTAACCACTGAGCCATAGCGCCGCCATTAAAATGTTAGCTTCTGTATAATTTGTTTTGGAATTCTTTTAAAATATTGTGCACAATAACTCATTTGATGCCACTTTACTTTAAAGTGTTATTTTAATAATTACAATCTTTCTGTTTTTCTCCCAGACTGTAACTGTAAAGGAAGCTGACATTCACCCCCAGAACCCTCCAAAGTTTGATAAAATTGAAGACATGGCAATGTTCACCTTCCTTCATGAGCCAGCCGTGCTGTTCAACCTCAAAGAGCGCTATGCAGCATGGATGATCTATGTAAGAGGAGAATGATTCGTTGTCCCTTGAAAATCGCATCCCAATTAGCTTCAATTACTGAACTGCATTTGTCCTTTCCCACAGACCTACTCAGGACTGTTTTGTGTCACTGTCAACCCCTACAAGTGGCTGCCGGTGTACAATCAGGAGGTGGTTGTAGCCTATAGAGGG[A/T]AAAAGAGGAGTGAAGCTCCTCCCCACATCTTTTCCATCTCTGATAACGCCTATCAGTACATGCTAACAGGTACGAAACAAATCCTCAAATCTGTTCTGCTTAGCAAATTCGAGAGCACCTCTCTTTTACCTGAAAGCATTAATCAAATCAGGCAATATATCTCATAAAGGGTAAAAAAAAAGTAGAATGTGTTGTGACTGACAAATCTCTGGATCAGTATTTCTCTGGTGAAAGACTAATAATCCAGAAGGCATGAAAATTAAAATAATAACTCAAGAATTAGTAACATTGCAGTATTTTCTATTTCAGACAGGGAAAATCAGTCAATTCTGATCACGTAAGTAAAATTTTTTTCCTTTTTAAGCAATTTCTTGGTTGCTTAAGTACTTTATGTGTTTTTTAACAGGACAGTTAACACACAAATTTAAATTCTGTTCTCATCCACTCGCTCTCCATTGTTGCAATCCTGTCCAAGTTTTTTCTTCTAATTAACACCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11779
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 307 | 1938 | 11 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23597598)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24610897 |
GRCz11 | 2 | 24266548 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATTTTTTCCCCTTGAAAYAGAGATGCTGCTCATCACCAACAACCCCTA[T/G]GACTACGCTTACATCTCCCAAGGAGAAACAACCGTAGCTTCAATTAAWGA
Long Flanking Sequence:
AAAGGTAATAAGTATCTTATGAAACATTTTAGCCATTAGTTATTTATAAGCCTTACTGACGTATTTTGAATTTATGCAATTTTTAATTTATCACTATTTCTCAAGATTATTTTTGATCTTTTTTTTTTAAGGGAAAATTCATCCGAATTCATTTTGGTGCCAGTGGAAAGTTGGCATCAGCTGACATTGAAACATGTGAGAATTCATTTGATTTAAACATCCAGACTCTATCTGGTAATACTGAGAATCAAAAATGAACATTTTTGTTTTTGTAAATACATCAGATCTTCTGGAGAAGTCAAGGGTGACTTTTCAGCTTAAAGCTGAAAGGGACTATCATATTTTCTACCAAATCCTCTCTCAGCGGAAACCTGAGCTGCTGGGTGAGATGCATTGGATATTCTGTATTCAAGAACCTTTTTCGGTATTAGCATTAAACAACAAACTGAAAAATTTTTTCCCCTTGAAACAGAGATGCTGCTCATCACCAACAACCCCTA[T/G]GACTACGCTTACATCTCCCAAGGAGAAACAACCGTAGCTTCAATTAATGATGGTGAAGAATTGCTTGCCACTGATGTAAGAATTAATTACATGACATCTTTGTCTTCCTCTCTCTGCAAGGTCTCAAATCACATCTCTTATTCTGTAAACTTTAGGAAGCGTTTGATGTACTAGGCTTCACTCAGGAGGAGAAAAATGGCATCTATAAATTGATTGGAGCCATTATGCACTTTGGCAATATGAAGTTCAAACAGAAGCAGAGGGAGGAGCAAGCAGAGGCTGATGGAACTGAAGGTGAATAGAGTATAATTCCTAAAGAAGCAAGCTAAAGGCAATATCATTTAGTCCATAATATTACATTCCCTCCAAATAGATAAATCTGATCTATTTCATAGATGGAGACAAAGTCGCATATCTGATGGGCCTAAACTCTGCTGACCTTATCAAGGGTCTGTGCCACCCAAGAGTCAAAGTAGGAAATGAGTGGGTCACCAAAGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7497
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 > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099532 | Missense | 596 | 1938 | 16 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23598926)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24609569 |
GRCz11 | 2 | 24265220 |
KASP Assay ID:
554-4055.1 (used for ordering genotyping assays)
KASP Sequence:
CCACTATGCTGGTACAGTTGACTATAATATCAACAACTGGCTGGTGAAGA[A/G]CAAAGACCCATTRAATGAGACTGTGGTGGGACTCTTTCAAAAGTCTACAG
Long Flanking Sequence:
ACTACAGTTTAACACCTTTGAGCAACTCTGCATCAACTTTACCAATGAGAAACTGCAACAGTTTTTCAACCACCACATGTTTGTGCTGGAACAAGAGGAGTACAAGAAAGAAGGGATTGAATGGGAGTTTATTGACTTTGGCATGGACTTGCAGGCCTGCATCGATCTCATTGAGAAAGTGAGTCACCAATTTGTGTCATTCTGACGCATTATGAACATTAAATTAAGTGATACAGTATATACTTTACATACTATACTTACTTTTCACTATCACACCTGATTGTTTCAGCCTATGGGCATCATGTCCATCCTTGAAGAGGAGTGCATGTTTCCCAAAGCAAGTGATTCAACCTTTAAAGCAAAGCTTTATGACAACCATCTTGGGAAATCAAATAACTTCCAGAAACCAAGAGCAATCAAAGGGAAGCCAGAGTCTCATTTTTCTCTGGTCCACTATGCTGGTACAGTTGACTATAATATCAACAACTGGCTGGTGAAGA[A/G]CAAAGACCCATTAAATGAGACTGTGGTGGGACTCTTTCAAAAGTCTACAGTCAAACTTCTGTCAATGCTCTTTGCTAACTATGCAGGGACAGAATCAGGTATGTCCAAGCTAAATTAGCCACGCTGGCACAATAGAATCTCATATGCAATCACAAGTGATTTAAGTGTTACAAGATTTAAGTAATTAATCTCTTATATTTTGACCATCTCAAGATAATGGTAAGGGAGGTAAAGGAGGTGGAAGTAAGAAGAAGGGCTCCTCCTTCCAGACTGTGTCTGCACTCCACAGGGTAATTGTAACTGTTGTGGACATGTTTAAAAAAAAATGTAGGAAACTGAAAATAGTTCTTAATCTCTTTGGTCTTAAATTCCACGTACATTTCTCCCTACAGGAAAACTTAAATAAGTTAATGACAAACCTAAGGTCAACTCACCCTCATTTTGTGCGCTGCATCATTCCTAATGAGACAAAGACTCCTGGTGCAATGGAGAATCCTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18019
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 942 | 1938 | 22 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23600534)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24607961 |
GRCz11 | 2 | 24263612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGAGCGACTTGAGGATGAGGAGSAGATGAATGCAGAGCTGAMAGCTAAG[A/T]AGAGAAAGCTGGAGGACGAATGCTCTGAGCTGMAGWAGGATATTGMTGAT
Long Flanking Sequence:
GAAAAAAATGTAACCTCTTCATAGGGATGCCCTACTGGTTATCCAGTGGAATGTCCGTGCCTTCATGGGGGTGAAAAATTGGCCCTGGATGAAGCTTTTCTTCAAGATAAAACCTCTTCTCAAGTCAGCAGAAGCAGAGAAAGAGATGGCAAATATGAAAGATGAATTTGCCAAGCTCAAAGAGGCTTATGCTAAATCCGAAGCGAGAAGGAAAGAGCTAGAAGAAAAAATGGTGTCTCTTCTCCAAGAGAAGAATGACCTACAACTTCAAGTTCAAGCGGTCAGTTAATATTTGCAACACATGTAGGTACATGAGTGTGTAGTATAGAAATCACTGTAATTTTACATATGTTTAAAAACAGGAGCAAGACAATCTCTGTGATGCAGAGGAACGATGTGACCAGCTCATCAAAAACAAGATTCAGCTTGAGGCTAAAGCCAAAGAGCTCACCGAGCGACTTGAGGATGAGGAGGAGATGAATGCAGAGCTGACAGCTAAG[A/T]AGAGAAAGCTGGAGGACGAATGCTCTGAGCTGAAGAAGGATATTGATGATCTGGAGCTCACTCTGGCTAAAGTCGAGAAAGAGAAGCATGCTACTGAGAACAAGGTCTGGTTTGCCTTTTTATACAAGCTCTTAGATGTACAAATTATTGCAAATTTAGCCCATCACATGGCATTGTTTTGGATGTATGTTAAGTTCTGTGCTATAAACGGATTTCTTTATCTTCAAATTTGGTCTTAAAGATGTCAGTGTGAATGCTAAATGAATGGGGACTAAATGTAATATTTCCCTTTTTTGTCTGGACCAAACAAACAAGAGATCAACCGTACAAGTGTAAAAACATCCTTAGTATGCATGTTCTTTTACAGGTAAAGAACCTGACAGAAGAAATGGCAGCTTTGGACGACATAATCGCAAAGCTGACCAAAGAGAAGAAAGCCTTGCAAGAAGCTCATCAGCAGACACTGGATGACCTGCAGAGTGAGGAGGACAAAGTCAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15964
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 954 | 1938 | 22 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23600570)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24607925 |
GRCz11 | 2 | 24263576 |
KASP Assay ID:
2259-1975.1 (used for ordering genotyping assays)
KASP Sequence:
AGCTGAMAGCTAAGWAGAGAAAGCTGGAGGACGAATGCTCTGAGCTGMAG[A/T]AGGATATTGMTGATCTGGAGCTCACTCTGGCTAAAGTCGAGAAAGAGAAG
Long Flanking Sequence:
GGTTATCCAGTGGAATGTCCGTGCCTTCATGGGGGTGAAAAATTGGCCCTGGATGAAGCTTTTCTTCAAGATAAAACCTCTTCTCAAGTCAGCAGAAGCAGAGAAAGAGATGGCAAATATGAAAGATGAATTTGCCAAGCTCAAAGAGGCTTATGCTAAATCCGAAGCGAGAAGGAAAGAGCTAGAAGAAAAAATGGTGTCTCTTCTCCAAGAGAAGAATGACCTACAACTTCAAGTTCAAGCGGTCAGTTAATATTTGCAACACATGTAGGTACATGAGTGTGTAGTATAGAAATCACTGTAATTTTACATATGTTTAAAAACAGGAGCAAGACAATCTCTGTGATGCAGAGGAACGATGTGACCAGCTCATCAAAAACAAGATTCAGCTTGAGGCTAAAGCCAAAGAGCTCACCGAGCGACTTGAGGATGAGGAGGAGATGAATGCAGAGCTGACAGCTAAGAAGAGAAAGCTGGAGGACGAATGCTCTGAGCTGAAG[A/T]AGGATATTGATGATCTGGAGCTCACTCTGGCTAAAGTCGAGAAAGAGAAGCATGCTACTGAGAACAAGGTCTGGTTTGCCTTTTTATACAAGCTCTTAGATGTACAAATTATTGCAAATTTAGCCCATCACATGGCATTGTTTTGGATGTATGTTAAGTTCTGTGCTATAAACGGATTTCTTTATCTTCAAATTTGGTCTTAAAGATGTCAGTGTGAATGCTAAATGAATGGGGACTAAATGTAATATTTCCCTTTTTTGTCTGGACCAAACAAACAAGAGATCAACCGTACAAGTGTAAAAACATCCTTAGTATGCATGTTCTTTTACAGGTAAAGAACCTGACAGAAGAAATGGCAGCTTTGGACGACATAATCGCAAAGCTGACCAAAGAGAAGAAAGCCTTGCAAGAAGCTCATCAGCAGACACTGGATGACCTGCAGAGTGAGGAGGACAAAGTCAACACCCTCACCAAGGCAAAAGCAAAGCTAGAGCAACAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25806
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 1169 | 1938 | 26 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23601868)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24606627 |
GRCz10 | 2 | 24623763 |
GRCz11 | 2 | 24262278 |
GRCz11 | 2 | 24279414 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGAGGCTGGAGGAGCTACAGCTGCTCAGATTGAGATGAATAAGAAA[C/T]GAGAGGCAGAGTTTCAGAAGCTCCGCAGAGACCTTGAAGAGGCCACTCTG
Long Flanking Sequence:
AGAAGGAGACTTGAAATTAACCCAGGAAAGCCTAATGGACCTGGAAAATGACAAGCAGCAGTTAGAGGAGCGTCTAAAAAAGTAAGGCAAAAACTCCCAATCTTTCACAGTCCGATCTGTTTGTTCATCACCAAGAACTTTACAATTATAAACACCCATTTCTATTTATAGGAAAGACTTTGAAATCAGTCAGCTCAATGGGAAAATCGAAGACGAACAAACTATTTGCATTCAGCTGCAGAAAAAACTGAAGGAACTTCAGGTAACAATTTAAAAAAATAGTGCATATTAACATTGAAATTTGAAATGAGTCAACCCTGGCATATTGTCATTACTAGGCACGTATTGAGGAGCTGGAGGAAGAGCTTGAGGCAGAAAGAGCTGCTAGAGCCAAAGTGGAGAAACAGAGAGCAGATTTAGCCAGAGAGCTGGAGGAGATCAGCGAGAGACTGGAGGAGGCTGGAGGAGCTACAGCTGCTCAGATTGAGATGAATAAGAAA[C/T]GAGAGGCAGAGTTTCAGAAGCTCCGCAGAGACCTTGAAGAGGCCACTCTGCAGCATGAGGCCACTGCCGCCACACTCAGGAAAAAACAAGCCGACAGTGTGGCTGAACTTGGAGAGCAGATAGACAATCTGCAGAGGGTCAAGCAAAAACTGGAGAAGGAGAAAAGTGAACTTAGGCTGGAGTTGGATGATGTAGTCTCAAACATGGAACATGTTGTAAAGACAAAGGTATTGTAAATACAAACACTCATAAAGAAAAATGAATGTTGCTTTTCTCAGCTAAAAAGTAATTCTTAGCCAAACTGTTTACCTTGTACAGGCAAATCTTGAGAAGATGACCAGATCTTTAGAAGACCAAATGAATGAATATAAAACAAAATATGAGGAAGGTCAGCGCTGCATTAATGACTTCACAATGCAGAAATCTAAACTACAATCTGAAAATGGTAAGATTAGTAAATAACATTCAATTAAATTATTTGAGCAACAGACCTCCAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25807
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 1174 | 1938 | 26 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23601883)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24606612 |
GRCz10 | 2 | 24623748 |
GRCz11 | 2 | 24262263 |
GRCz11 | 2 | 24279399 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCTACAGCTGCTCAGATTGAGATGAATAAGAAACGAGAGGCAGAGTTT[C/T]AGAAGCTCCGCAGAGACCTTGAAGAGGCCACTCTGCAGCATGAGGCCACT
Long Flanking Sequence:
ATTAACCCAGGAAAGCCTAATGGACCTGGAAAATGACAAGCAGCAGTTAGAGGAGCGTCTAAAAAAGTAAGGCAAAAACTCCCAATCTTTCACAGTCCGATCTGTTTGTTCATCACCAAGAACTTTACAATTATAAACACCCATTTCTATTTATAGGAAAGACTTTGAAATCAGTCAGCTCAATGGGAAAATCGAAGACGAACAAACTATTTGCATTCAGCTGCAGAAAAAACTGAAGGAACTTCAGGTAACAATTTAAAAAAATAGTGCATATTAACATTGAAATTTGAAATGAGTCAACCCTGGCATATTGTCATTACTAGGCACGTATTGAGGAGCTGGAGGAAGAGCTTGAGGCAGAAAGAGCTGCTAGAGCCAAAGTGGAGAAACAGAGAGCAGATTTAGCCAGAGAGCTGGAGGAGATCAGCGAGAGACTGGAGGAGGCTGGAGGAGCTACAGCTGCTCAGATTGAGATGAATAAGAAACGAGAGGCAGAGTTT[C/T]AGAAGCTCCGCAGAGACCTTGAAGAGGCCACTCTGCAGCATGAGGCCACTGCCGCCACACTCAGGAAAAAACAAGCCGACAGTGTGGCTGAACTTGGAGAGCAGATAGACAATCTGCAGAGGGTCAAGCAAAAACTGGAGAAGGAGAAAAGTGAACTTAGGCTGGAGTTGGATGATGTAGTCTCAAACATGGAACATGTTGTAAAGACAAAGGTATTGTAAATACAAACACTCATAAAGAAAAATGAATGTTGCTTTTCTCAGCTAAAAAGTAATTCTTAGCCAAACTGTTTACCTTGTACAGGCAAATCTTGAGAAGATGACCAGATCTTTAGAAGACCAAATGAATGAATATAAAACAAAATATGAGGAAGGTCAGCGCTGCATTAATGACTTCACAATGCAGAAATCTAAACTACAATCTGAAAATGGTAAGATTAGTAAATAACATTCAATTAAATTATTTGAGCAACAGACCTCCAACAATGATAAAATACATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19752
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 1225 | 1938 | 26 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23602036)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24606459 |
GRCz11 | 2 | 24262110 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATAGACAATCTGCAGAGGGTCAAGCAAAAACTGGAGAAGGAGAAAAGT[G/T]AACTTAGGCTGGAGTTGGATGATGTAGTCTCAAACATGGAACATGTTGTA
Long Flanking Sequence:
TAGGAAAGACTTTGAAATCAGTCAGCTCAATGGGAAAATCGAAGACGAACAAACTATTTGCATTCAGCTGCAGAAAAAACTGAAGGAACTTCAGGTAACAATTTAAAAAAATAGTGCATATTAACATTGAAATTTGAAATGAGTCAACCCTGGCATATTGTCATTACTAGGCACGTATTGAGGAGCTGGAGGAAGAGCTTGAGGCAGAAAGAGCTGCTAGAGCCAAAGTGGAGAAACAGAGAGCAGATTTAGCCAGAGAGCTGGAGGAGATCAGCGAGAGACTGGAGGAGGCTGGAGGAGCTACAGCTGCTCAGATTGAGATGAATAAGAAACGAGAGGCAGAGTTTCAGAAGCTCCGCAGAGACCTTGAAGAGGCCACTCTGCAGCATGAGGCCACTGCCGCCACACTCAGGAAAAAACAAGCCGACAGTGTGGCTGAACTTGGAGAGCAGATAGACAATCTGCAGAGGGTCAAGCAAAAACTGGAGAAGGAGAAAAGT[G/T]AACTTAGGCTGGAGTTGGATGATGTAGTCTCAAACATGGAACATGTTGTAAAGACAAAGGTATTGTAAATACAAACACTCATAAAGAAAAATGAATGTTGCTTTTCTCAGCTAAAAAGTAATTCTTAGCCAAACTGTTTACCTTGTACAGGCAAATCTTGAGAAGATGACCAGATCTTTAGAAGACCAAATGAATGAATATAAAACAAAATATGAGGAAGGTCAGCGCTGCATTAATGACTTCACAATGCAGAAATCTAAACTACAATCTGAAAATGGTAAGATTAGTAAATAACATTCAATTAAATTATTTGAGCAACAGACCTCCAACAATGATAAAATACATGATCATACGTTTAGGTGAACTTTCAAGACAGCTGGAGGAAAAGGACTCTCTTGTCTCCCAGCTAACCAGAAGCAAGATGTCTTACACTCAGCAAATTGAAGATCTTAAAAGACAACTGGAGGAGGAAACAAAGGTGTGAATTGAGTTTAAAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19753
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099532 | Splice Site, Nonsense | 1392 | 1938 | 29 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23602792)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24605703 |
GRCz11 | 2 | 24261354 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAGTACGAAACTGATGCCATCCAGAGAACTGAAGAACTGGAGGAAGCC[A/T]AGTAAGATCTGTTTCTATAAAATATTTCATACAAATTCTTCTTTAAGGTT
Long Flanking Sequence:
TCTAAACTACAATCTGAAAATGGTAAGATTAGTAAATAACATTCAATTAAATTATTTGAGCAACAGACCTCCAACAATGATAAAATACATGATCATACGTTTAGGTGAACTTTCAAGACAGCTGGAGGAAAAGGACTCTCTTGTCTCCCAGCTAACCAGAAGCAAGATGTCTTACACTCAGCAAATTGAAGATCTTAAAAGACAACTGGAGGAGGAAACAAAGGTGTGAATTGAGTTTAAAATTCTTTTTTAATTATTTGCCATCATTTTTTTGGTCTGTTAAATAATTATGCAACCTCCTCCAGGCAAAAAGCGCTCTCGCCCATGCTGTACAGTCAGCCCGTCATGACACAGATCTGCTTAGAGAGCAGTATGAGGAGGAGCAGGAAGCTAAAGCAGAGCTACAGCGAGGCATGTCCAAAGCTAATTCTGAGGTGGCACAGTGGAGAACCAAGTACGAAACTGATGCCATCCAGAGAACTGAAGAACTGGAGGAAGCC[A/T]AGTAAGATCTGTTTCTATAAAATATTTCATACAAATTCTTCTTTAAGGTTTAACTTCTCTACTGACAGAGAAGCTTTTTGTTTGTGTTATGTTTATTTTCAAATGTAAGACGAACAAAAAGTTTTTCTGTTAGTAGGCCAAGCTTCCCTAAACAGAAGGTAACACTATAATAACACGTCAATCATTTTCGTGTAGGTGTGCACTAAAAAAGTATCTTCCCCAAAAATCTTCTTTAATTTTCTATAACAGAAAGAAACTGGCTCAACGCTTACAGGAAACCGAAGAAGCTGTTGAAGCAGTAAATGCAAAGTGTTCATCTCTTGAAAAGACCAAACACAGACTCCAAAATGAGATTGAAGATCTTATGGTGGACCTGGAGAGGTCTAATGCGGCTGCTGCAGCCTTAGACAAAAAGCAAAGAAACTTTGATAAGGTAATCAAACATAGTTCCTATATTAGCCATAACCGTAGTTTCTAAATACCTCTAATACTAAAATTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5139
Status:
F2 line generated
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099532 | Splice Site, Nonsense | 1393 | 1938 | 30 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23603043)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24605452 |
GRCz11 | 2 | 24261103 |
KASP Assay ID:
554-3543.1 (used for ordering genotyping assays)
KASP Sequence:
CACTAAAAAAGTATCTTNCCCAAAAATCTTCTTTWATTTTCTATAACAGA[A/T]AGAAACTGGCTCAACGCTTACAGGAAACCGAAGAAGCTGTTGAAGCAGTA
Long Flanking Sequence:
AATTATTTGCCATCATTTTTTTGGTCTGTTAAATAATTATGCAACCTCCTCCAGGCAAAAAGCGCTCTCGCCCATGCTGTACAGTCAGCCCGTCATGACACAGATCTGCTTAGAGAGCAGTATGAGGAGGAGCAGGAAGCTAAAGCAGAGCTACAGCGAGGCATGTCCAAAGCTAATTCTGAGGTGGCACAGTGGAGAACCAAGTACGAAACTGATGCCATCCAGAGAACTGAAGAACTGGAGGAAGCCAAGTAAGATCTGTTTCTATAAAATATTTCATACAAATTCTTCTTTAAGGTTTAACTTCTCTACTGACAGAGAAGCTTTTTGTTTGTGTTATGTTTATTTTCAAATGTAAGACGAACAAAAAGTTTTTCTGTTAGTAGGCCAAGCTTCCCTAAACAGAAGGTAACACTATAATAACACGTCAATCATTTTCGTGTAGGTGTGCACTAAAAAAGTATCTTCCCCAAAAATCTTCTTTAATTTTCTATAACAGA[A/T]AGAAACTGGCTCAACGCTTACAGGAAACCGAAGAAGCTGTTGAAGCAGTAAATGCAAAGTGTTCATCTCTTGAAAAGACCAAACACAGACTCCAAAATGAGATTGAAGATCTTATGGTGGACCTGGAGAGGTCTAATGCGGCTGCTGCAGCCTTAGACAAAAAGCAAAGAAACTTTGATAAGGTAATCAAACATAGTTCCTATATTAGCCATAACCGTAGTTTCTAAATACCTCTAATACTAAAATTTGCTTACATAAAAAACACAGGTACTGTCTGAGTGGAAGCAGAAGTTTGAAGAGTCGCAAGCCGAGTTAGAGAGCTCTCAGAAAGAAGCAAGATGTCTTAGCACTGAACTTTTCAAGCTGAAGAACTCCTATGAGGAAGCTTTAGATCACCTGGAGACCATGAAGAGAGAAAATAAAAATCTCCAAGGTGAATAAAAAGATTACCAACACAAAAACACTGTGTTTTTCTAAATCAACTAAAATAGATACATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32912
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 1592 | 1938 | 33 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23604844)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24603651 |
GRCz11 | 2 | 24259302 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGCAAACTAGCCGAGAAGGATGAAGAGATGGAGCAGAGCAAACGCAATT[T/A]GCAGAGGACCATTGACACTCTGCAAAGCTCCTTGGAGTCAGAAACCAGAA
Long Flanking Sequence:
GGATAACTTTATTTATTTTGGATTGTGAAAGTAAAATTCTCCTACGAGAGTGATTATATCGCCTCCCGATGGTGAATGCGGTTATACTCACGGCAGGTATTATTTGATAATTCAGTTGTTTATTTCACTGATTTGGCAACCGTCAAACGTCGTCAGGGAAACAGTTTGAATATCTGCTTAGTAAAAGAACATTAGTGTGCCATTTGGGAAGACACTACATACATATACTATACTGTTGAGTGTGTAAGTGCATAAGTACATAGTGCATAAGTGCATAGTGTATAGTGTGCCATTTGGGATGCAGCTATTATCGTTGTTGTTGTTAAAACAGAATAATGTATTGCAAAGCCATAGATCACATTCTTCTGCTTGAAAGGCATCACTGGAGCACGAGGAGGGTAAGATTCTGCGAGCCCAGCTGGAGTTCAGCCAAATTAAGGCTGATATCGAGCGCAAACTAGCCGAGAAGGATGAAGAGATGGAGCAGAGCAAACGCAATT[T/A]GCAGAGGACCATTGACACTCTGCAAAGCTCCTTGGAGTCAGAAACCAGAAGCAGAAATGAGGCCCTCAGAATAAAAAAGAAGATGGAGGGCGACCTGAATGAGATGGAGATCCAGCTTAGTCAGGCAAACCGACAAGCAGCAGAGGCCCAAAAACAACTTAAGAGTGTGCATGCACATATGAAAGTAAGACAAACACTGGACTAATACTGCAAAGATTTCTGGAGGGTTGTTTAAATGATTTTCTTCCCCTCAACTATTTAGGATGCTCAGCTTCAGCTGGACGACTCCCTGAGAACAAATGAAGATCTTAAGGAGAACACAGCCATTGTAGAGAGACGCAACAACCTTCTGCAGGCTGAACTAGAGGAACTCAGAGCAGCTCTTGAGCAAACCGAAAGAGGCCGTAAGCTTGCTGAGCAGGAGCTTCTGGATACCAGTGAAAGAGTACAGCTGCTGCACTCCCAGGTATGCTAAATGTTTAGTTACTCTTTATTTTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32913
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 1619 | 1938 | 33 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23604924)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24603571 |
GRCz11 | 2 | 24259222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTGGAGTCAGAAACCAGAAGCAGAAATGAGGCCCTCAGAATAAAAAAG[A/T]AGATGGAGGGCGACCTGAATGAGATGGAGATCCAGCTTAGTCAGGCAAAC
Long Flanking Sequence:
GTTATACTCACGGCAGGTATTATTTGATAATTCAGTTGTTTATTTCACTGATTTGGCAACCGTCAAACGTCGTCAGGGAAACAGTTTGAATATCTGCTTAGTAAAAGAACATTAGTGTGCCATTTGGGAAGACACTACATACATATACTATACTGTTGAGTGTGTAAGTGCATAAGTACATAGTGCATAAGTGCATAGTGTATAGTGTGCCATTTGGGATGCAGCTATTATCGTTGTTGTTGTTAAAACAGAATAATGTATTGCAAAGCCATAGATCACATTCTTCTGCTTGAAAGGCATCACTGGAGCACGAGGAGGGTAAGATTCTGCGAGCCCAGCTGGAGTTCAGCCAAATTAAGGCTGATATCGAGCGCAAACTAGCCGAGAAGGATGAAGAGATGGAGCAGAGCAAACGCAATTTGCAGAGGACCATTGACACTCTGCAAAGCTCCTTGGAGTCAGAAACCAGAAGCAGAAATGAGGCCCTCAGAATAAAAAAG[A/T]AGATGGAGGGCGACCTGAATGAGATGGAGATCCAGCTTAGTCAGGCAAACCGACAAGCAGCAGAGGCCCAAAAACAACTTAAGAGTGTGCATGCACATATGAAAGTAAGACAAACACTGGACTAATACTGCAAAGATTTCTGGAGGGTTGTTTAAATGATTTTCTTCCCCTCAACTATTTAGGATGCTCAGCTTCAGCTGGACGACTCCCTGAGAACAAATGAAGATCTTAAGGAGAACACAGCCATTGTAGAGAGACGCAACAACCTTCTGCAGGCTGAACTAGAGGAACTCAGAGCAGCTCTTGAGCAAACCGAAAGAGGCCGTAAGCTTGCTGAGCAGGAGCTTCTGGATACCAGTGAAAGAGTACAGCTGCTGCACTCCCAGGTATGCTAAATGTTTAGTTACTCTTTATTTTGAACAGATCAATTACACAAAACGTTTTTCCAAATTAATCCCAATGAATCTTCGGCCAGAACACAAGCCTGTTAAATCAGAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5718
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 1691 | 1938 | 34 | 39 |
ENSDART00000099532 | Nonsense | 1691 | 1938 | 34 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23605218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24603277 |
GRCz11 | 2 | 24258928 |
KASP Assay ID:
554-3047.1 (used for ordering genotyping assays)
KASP Sequence:
CCATTGTAGAGAGACGCAACAACCTTCTGCAGGCTGAACTAGAGGAACTC[A/T]GAGCAGCTCTTGAGCAAACCGAAAGAGGCCGTAAGCTTGCTGAGCAGGAG
Long Flanking Sequence:
AGGCATCACTGGAGCACGAGGAGGGTAAGATTCTGCGAGCCCAGCTGGAGTTCAGCCAAATTAAGGCTGATATCGAGCGCAAACTAGCCGAGAAGGATGAAGAGATGGAGCAGAGCAAACGCAATTTGCAGAGGACCATTGACACTCTGCAAAGCTCCTTGGAGTCAGAAACCAGAAGCAGAAATGAGGCCCTCAGAATAAAAAAGAAGATGGAGGGCGACCTGAATGAGATGGAGATCCAGCTTAGTCAGGCAAACCGACAAGCAGCAGAGGCCCAAAAACAACTTAAGAGTGTGCATGCACATATGAAAGTAAGACAAACACTGGACTAATACTGCAAAGATTTCTGGAGGGTTGTTTAAATGATTTTCTTCCCCTCAACTATTTAGGATGCTCAGCTTCAGCTGGACGACTCCCTGAGAACAAATGAAGATCTTAAGGAGAACACAGCCATTGTAGAGAGACGCAACAACCTTCTGCAGGCTGAACTAGAGGAACTC[A/T]GAGCAGCTCTTGAGCAAACCGAAAGAGGCCGTAAGCTTGCTGAGCAGGAGCTTCTGGATACCAGTGAAAGAGTACAGCTGCTGCACTCCCAGGTATGCTAAATGTTTAGTTACTCTTTATTTTGAACAGATCAATTACACAAAACGTTTTTCCAAATTAATCCCAATGAATCTTCGGCCAGAACACAAGCCTGTTAAATCAGAAGAAGAAGCTGGAGACGGATATATCCCAGCTTCAGACAGAAGTGGAAGAGGCAGTGCAAGAATGCAGGAATGCTGAGGAAAAAGCCAAGAAGGCCATCACTGATGCTGCCATGATGGCGGAGGAGCTGAAGAAGGAGCAGGATACAAGTGCTCACCTGGAGAGGATGAAGAAGAACATGGAGCAGACCATTAAAGACCTGCAGCATCGCCTGGATGAAGCAGAACAAATCGCTATGAAGGGAGGCAAGAAACAAGTCCAGAAACTGGAGGCCAGGGTGAGTGAATTAACATCAATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2053
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 1691 | 1938 | 34 | 39 |
ENSDART00000099532 | Nonsense | 1691 | 1938 | 34 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23605218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24603277 |
GRCz11 | 2 | 24258928 |
KASP Assay ID:
554-3047.1 (used for ordering genotyping assays)
KASP Sequence:
CCATTGTAGAGAGACGCAACAACCTTCTGCAGGCTGAACTAGAGGAACTC[A/T]GAGCAGCTCTTGAGCAAACCGAAAGAGGCCGTAAGCTTGCTGAGCAGGAG
Long Flanking Sequence:
AGGCATCACTGGAGCACGAGGAGGGTAAGATTCTGCGAGCCCAGCTGGAGTTCAGCCAAATTAAGGCTGATATCGAGCGCAAACTAGCCGAGAAGGATGAAGAGATGGAGCAGAGCAAACGCAATTTGCAGAGGACCATTGACACTCTGCAAAGCTCCTTGGAGTCAGAAACCAGAAGCAGAAATGAGGCCCTCAGAATAAAAAAGAAGATGGAGGGCGACCTGAATGAGATGGAGATCCAGCTTAGTCAGGCAAACCGACAAGCAGCAGAGGCCCAAAAACAACTTAAGAGTGTGCATGCACATATGAAAGTAAGACAAACACTGGACTAATACTGCAAAGATTTCTGGAGGGTTGTTTAAATGATTTTCTTCCCCTCAACTATTTAGGATGCTCAGCTTCAGCTGGACGACTCCCTGAGAACAAATGAAGATCTTAAGGAGAACACAGCCATTGTAGAGAGACGCAACAACCTTCTGCAGGCTGAACTAGAGGAACTC[A/T]GAGCAGCTCTTGAGCAAACCGAAAGAGGCCGTAAGCTTGCTGAGCAGGAGCTTCTGGATACCAGTGAAAGAGTACAGCTGCTGCACTCCCAGGTATGCTAAATGTTTAGTTACTCTTTATTTTGAACAGATCAATTACACAAAACGTTTTTCCAAATTAATCCCAATGAATCTTCGGCCAGAACACAAGCCTGTTAAATCAGAAGAAGAAGCTGGAGACGGATATATCCCAGCTTCAGACAGAAGTGGAAGAGGCAGTGCAAGAATGCAGGAATGCTGAGGAAAAAGCCAAGAAGGCCATCACTGATGCTGCCATGATGGCGGAGGAGCTGAAGAAGGAGCAGGATACAAGTGCTCACCTGGAGAGGATGAAGAAGAACATGGAGCAGACCATTAAAGACCTGCAGCATCGCCTGGATGAAGCAGAACAAATCGCTATGAAGGGAGGCAAGAAACAAGTCCAGAAACTGGAGGCCAGGGTGAGTGAATTAACATCAATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18728
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 1918 | 1938 | 38 | 39 |
ENSDART00000099532 | Nonsense | 1918 | 1938 | 38 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23606440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24602055 |
GRCz11 | 2 | 24257706 |
KASP Assay ID:
2259-1982.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGCATGAGCTTGATGAGGCAGAAGAAAGAGCTGACATTGCAGAGTCA[C/T]AAGTCAATAAGCTACGTGCCAAAAGTCGTGATGTCAGTTCTAAGGTCAGT
Long Flanking Sequence:
CTAACTAAAGAACTAACAGGAACTAACATTATTTAATTTAAATAATGTTAACAAAGATAAATAAATACCATAATAGACGTGTTAATCATTTTTTGTTCATATTATTAAATACATTAACTCACATTAACTAATGGACCATTATTTTATTATGTTACCTACATATTGAAAGTGTAACGACTCGACACTTTCCCACATGAAATTCTCATCTGCGTTTTCTATATTTTCTTTTGAAGACTGAGGAGGACCGCAAGAATCTGGCTCGTCTGCAAGATCTGGTTGACAAGCTTCAGCTAAAGGTTAAAGCTTACAAGAGGGCTGCAGAGGAAGCTGTAAGTATTGGCCAAAATATCACACATTTTTGCTAATAAATTGTACTCTACAGTCTCAGAACTGCTAATCCTGCTTTACAGGAGGAACAAGCCAACACTAATCTTAGCAAGTTCCGGAAAATCCAGCATGAGCTTGATGAGGCAGAAGAAAGAGCTGACATTGCAGAGTCA[C/T]AAGTCAATAAGCTACGTGCCAAAAGTCGTGATGTCAGTTCTAAGGTCAGTTACACTTATAGCTGTCATGCTCCAATCAAGATTTAACACCTCTCATTTACAAGTACAATAACACAAGGTTCTCAACTAAATAAAATCTACATTATAGATACATACACTACCAGATAAAATTCTCGTAGTTGATCCCAGTTTTAAAAGCAACAAATAATAACTTGAATTCTAGGAAAAGTGGCAGAAGGTAGATTTTTCAAATCAGTCATCTGTTGAACTGCATTCCAATCATCACACATACTGCAGAAGATTTAGTAGAACCTGCATGGACCCAAGATTCTCACAGAAATCAGTCAAGTTTGGTAAAGGAAAAATCATAGTTTAGGGTTACAGTACATTCAGTATGGATGAGATCTACAGAGTGGATGGCACTTTCTTCAGCTGGATAGTACTCTGTCTCATACTTCAGCCTCCACATCAAAGTTCCTGAACGCAATGAAGGTCAAGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10912
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 |
---|---|---|---|---|---|
ENSDART00000099532 | Nonsense | 1918 | 1938 | 38 | 39 |
ENSDART00000099532 | Nonsense | 1918 | 1938 | 38 | 39 |
Genomic Location (Zv9):
Chromosome 2 (position 23606440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 24602055 |
GRCz11 | 2 | 24257706 |
KASP Assay ID:
2259-1982.1 (used for ordering genotyping assays)
KASP Sequence:
TCCAGCATGAGCTWGATGAGGCAGAAGAAAGAGCTGACATTGCAGAGTCA[C/T]AAGTCAATAAGCTACGTGCCAAAAGTCGTGATGTCAGTTCTAAGGTCAGT
Long Flanking Sequence:
CTAACTAAAGAACTAACAGGAACTAACATTATTTAATTTAAATAATGTTAACAAAGATAAATAAATACCATAATAGACGTGTTAATCATTTTTTGTTCATATTATTAAATACATTAACTCACATTAACTAATGGACCATTATTTTATTATGTTACCTACATATTGAAAGTGTAACGACTCGACACTTTCCCACATGAAATTCTCATCTGCGTTTTCTATATTTTCTTTTGAAGACTGAGGAGGACCGCAAGAATCTGGCTCGTCTGCAAGATCTGGTTGACAAGCTTCAGCTAAAGGTTAAAGCTTACAAGAGGGCTGCAGAGGAAGCTGTAAGTATTGGCCAAAATATCACACATTTTTGCTAATAAATTGTACTCTACAGTCTCAGAACTGCTAATCCTGCTTTACAGGAGGAACAAGCCAACACTAATCTTAGCAAGTTCCGGAAAATCCAGCATGAGCTTGATGAGGCAGAAGAAAGAGCTGACATTGCAGAGTCA[C/T]AAGTCAATAAGCTACGTGCCAAAAGTCGTGATGTCAGTTCTAAGGTCAGTTACACTTATAGCTGTCATGCTCCAATCAAGATTTAACACCTCTCATTTACAAGTACAATAACACAAGGTTCTCAACTAAATAAAATCTACATTATAGATACATACACTACCAGATAAAATTCTCGTAGTTGATCCCAGTTTTAAAAGCAACAAATAATAACTTGAATTCTAGGAAAAGTGGCAGAAGGTAGATTTTTCAAATCAGTCATCTGTTGAACTGCATTCCAATCATCACACATACTGCAGAAGATTTAGTAGAACCTGCATGGACCCAAGATTCTCACAGAAATCAGTCAAGTTTGGTAAAGGAAAAATCATAGTTTAGGGTTACAGTACATTCAGTATGGATGAGATCTACAGAGTGGATGGCACTTTCTTCAGCTGGATAGTACTCTGTCTCATACTTCAGCCTCCACATCAAAGTTCCTGAACGCAATGAAGGTCAAGGTG
Associated Phenotype:
Not determined