Busch Lab

ZMP

vmhc

Ensembl ID:
ENSDARG00000079564
ZFIN ID:
ZDB-GENE-991123-5
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]
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]

Alleles

There are 22 alleles of this gene:

Allele Name Consequence Status Availability
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
sa18019 Nonsense Available for shipment Available now
sa15964 Nonsense Available for shipment Available now
sa19752 Nonsense Available for shipment Available now
sa19753 Splice Site, Nonsense Available for shipment Available now
sa10912 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa10407
Status:
Available for shipment
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Availability:
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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.
Availability:
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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.
Availability:
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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.
Availability:
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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:
sa18019
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
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.
Availability:
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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:
sa19752
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
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.
Availability:
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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:
sa10912
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
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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