Busch Lab

ZMP

myhz2

Ensembl ID:
ENSDARG00000012944
ZFIN ID:
ZDB-GENE-020604-1
Description:
myosin, heavy polypeptide 2, fast muscle specific [Source:RefSeq peptide;Acc:NP_694514]
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 8 alleles of this gene:

Allele Name Consequence Status Availability
sa40473 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa40474 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa26505 Nonsense Mutation detected in F1 DNA Not yet available
sa8989 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa6986 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa26506 Nonsense Mutation detected in F1 DNA Not yet available
sa10296 Essential Splice Site Available for shipment Available now
sa40475 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa40473
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051361 None None 1935 None 40
ENSDART00000124498 Essential Splice Site None 452 2 14
ENSDART00000126873 Essential Splice Site None 1935 2 41
ENSDART00000128949 Essential Splice Site None 966 2 23
Genomic Location (Zv9):
Chromosome 5 (position 33844130)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31606362
GRCz11 5 32206515
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAATTCTTTGATTGAGGATTAATACATTGTATGCTGTTTTTTTATTGA[A/G]GGGTAGTGAATTATTCATCTGGTCTCAAGGAACGCAAGGTAAGATTTTGG
Long Flanking Sequence:
AAATATTCTATGGAATACCTCATCCTAAAAAGGATTTAATGGCTTAAGTGCACGTCAAATGGCAATATATTAATAGAGTAAAATAAATATTTGTAAATGAACAAGTTAATTAGCTGCAGTGATGCTCAATCAAAATAACACCCGAGATAGAGGCTGTGAACCTAATAATTGGGGATATTTTAACAAGTATAGGTTTGACTTATGACAGATACCACCAGTTATAGGCTATCTGTGAGTCTGTCCTCAACTTGCTCATAAAATGGGTCAAGAAAGCCGATCATAAATCAGAAGGTTTGGGCTTGCCCATGTATAGATTTTGCTTACTGTGCATGGTCAACTTCAATAAAAGCCCAGTGGAGAGAGCAGAAGGGCTGCAGAGGAGACCTCAGACGTTCCTGCCAGTGGTAAGAGCTCATGCTGGCTGTGACTGTACCTAAAGTTAATTGAGTTTTAAATTCTTTGATTGAGGATTAATACATTGTATGCTGTTTTTTTATTGA[A/G]GGGTAGTGAATTATTCATCTGGTCTCAAGGAACGCAAGGTAAGATTTTGGGTAGAGCTTGTTTATTTGTGAGAAGATATCTAAAGCATGCTGCATTTAAATAACTTAAACAAAGATGTTTTAATTAAGAAAATTCAATTTGAATTAAATTAGATTTTTAAAGCTCTTTTCACAATAACTATCACCTTTACAAAAGGTGAATGTTATTACATCACAATCAAAATGAGTTAAGGTGTAACTAACCTTAATAACAATGAATACATTGTTAATAAAGTGATCTAATCATTACAACAATTAAGAACAATTTACAAAAATCTAATCTATTTTGGGATCTGTATCTGTATCTATTTACAGATACTCTATATGCACCTAAAAATATTGTAGTAGTAGGATAATTCTAGGGATTAGGTGCATTGTGTTGTTTAGTACAAAGCACTGAAGGTGCACTTAACATAATAGCTTTTTAATGTCTCATATTATAGTCATGTTTTTGTTCCACTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40474
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051361 Essential Splice Site 118 1935 4 40
ENSDART00000124498 Essential Splice Site 118 452 5 14
ENSDART00000126873 Essential Splice Site 118 1935 5 41
ENSDART00000128949 Essential Splice Site 118 966 5 23
Genomic Location (Zv9):
Chromosome 5 (position 33845989)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31608221
GRCz11 5 32208374
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACATTTAGTCTGTGTGTTTGCCATCTGTTCACTTCTCTCCTCATTTC[A/T]GACCTACTCTGGGCTGTTCTGCGCCACTGTAAACCCCTACAAGTGGCTCC
Long Flanking Sequence:
AAGCCTGAGAAGGAGAGAATTGAAGCTCAGAGCAAACCATTTGATGCCAAAACCGCTTGTTATGTGGTTGATGACAAAGAGCTGTACGTCAAGGGAACAATCAAGAGCAAAGATGGTGGCAAAGTCACTGTTGTTACACTTGACACTCAGACGGTAATTTTACTCTTGCAATTCAAGCAGTTGTTATTTACACGCTAGAATGCTTTTTTAAAATTTTGTTTTAGTTATTTATTTTGCATTCATGTAAACACTTTCTTTTTATTTAAATTTATAGGAGAAAGTTGTTAAGGAGGATGATGTCCACCCAATGAATCCTCCCAAGTTTGACAAGATTGAGGACATGGCCATGATGACCCATCTCAATGAACCCTCTGTGCTGTATAACCTCAAAGAGCGTTATGCAGCATGGATGATCTACGTAAGTTCTGAAACAACCTAAAACAGCACTGCAAGACATTTAGTCTGTGTGTTTGCCATCTGTTCACTTCTCTCCTCATTTC[A/T]GACCTACTCTGGGCTGTTCTGCGCCACTGTAAACCCCTACAAGTGGCTCCCAGTGTATGACGCAGAAGTGGTTGCTGCCTACAGAGGCAAGAAGCGTATGGAGGCTCCACCCCACATCTTCTCTGTCTCTGACAACGCCTATCAGTTCATGTTGACTGGTGAGATTACAACATCTGAATTACAAAATTCTGAAGTTCACATTCATCATTTTAACAAAACAATTGCTAAAACATTATTACCTTTGCATTTACAGACAGAGAGAACCAGTCTGTCCTGATTACGTATGTATCTAATCTAATTGAGATGCTGAGAACAGGTTTAGTTTCAACTTGTGCAACTTCTACATGTCTTATCATTTTATGTCTTCTTGTCTCTCATAAACCAGTGGAGAATCTGGTGCTGGAAAGACTGTGAACACCAAACGTGTCATCCAGTACTTTGCCACCGTTGCAGTTCAGGGCGGTGACAAGAAGAAAGAGCAAGCTGCTGGCAAAATGCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26505
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051361 Nonsense 136 1935 4 40
ENSDART00000124498 Nonsense 136 452 5 14
ENSDART00000126873 Nonsense 136 1935 5 41
ENSDART00000128949 Nonsense 136 966 5 23
Genomic Location (Zv9):
Chromosome 5 (position 33846047)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31608279
GRCz11 5 32208432
KASP Assay ID:
2259-6039.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGGGCTGTTCTGCGCCACTGTAAACCCCTACAAGTGGCTCCCAGTGTA[T/G]GACGCAGAAGTGGTTGCTGCCTACAGAGGCAAGAAGCGTATGGAGGCTCC
Long Flanking Sequence:
GTTATGTGGTTGATGACAAAGAGCTGTACGTCAAGGGAACAATCAAGAGCAAAGATGGTGGCAAAGTCACTGTTGTTACACTTGACACTCAGACGGTAATTTTACTCTTGCAATTCAAGCAGTTGTTATTTACACGCTAGAATGCTTTTTTAAAATTTTGTTTTAGTTATTTATTTTGCATTCATGTAAACACTTTCTTTTTATTTAAATTTATAGGAGAAAGTTGTTAAGGAGGATGATGTCCACCCAATGAATCCTCCCAAGTTTGACAAGATTGAGGACATGGCCATGATGACCCATCTCAATGAACCCTCTGTGCTGTATAACCTCAAAGAGCGTTATGCAGCATGGATGATCTACGTAAGTTCTGAAACAACCTAAAACAGCACTGCAAGACATTTAGTCTGTGTGTTTGCCATCTGTTCACTTCTCTCCTCATTTCAGACCTACTCTGGGCTGTTCTGCGCCACTGTAAACCCCTACAAGTGGCTCCCAGTGTA[T/G]GACGCAGAAGTGGTTGCTGCCTACAGAGGCAAGAAGCGTATGGAGGCTCCACCCCACATCTTCTCTGTCTCTGACAACGCCTATCAGTTCATGTTGACTGGTGAGATTACAACATCTGAATTACAAAATTCTGAAGTTCACATTCATCATTTTAACAAAACAATTGCTAAAACATTATTACCTTTGCATTTACAGACAGAGAGAACCAGTCTGTCCTGATTACGTATGTATCTAATCTAATTGAGATGCTGAGAACAGGTTTAGTTTCAACTTGTGCAACTTCTACATGTCTTATCATTTTATGTCTTCTTGTCTCTCATAAACCAGTGGAGAATCTGGTGCTGGAAAGACTGTGAACACCAAACGTGTCATCCAGTACTTTGCCACCGTTGCAGTTCAGGGCGGTGACAAGAAGAAAGAGCAAGCTGCTGGCAAAATGCAGGTATGAGTTTAAAACTCTAGAAAATATTGCTAAAAAAATGTTTAGAAATTTAATGGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8989
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051361 Essential Splice Site 423 1935 12 40
ENSDART00000124498 Essential Splice Site 423 452 13 14
ENSDART00000126873 Essential Splice Site 423 1935 13 41
ENSDART00000128949 Essential Splice Site 423 966 13 23
Genomic Location (Zv9):
Chromosome 5 (position 33847663)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31609895
GRCz11 5 32210048
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTSAAGGTCGGAAATGAGTTTGTGACCAAAGGACAGACTGTGCCACAG[G/A]TATGYAGTAACATTTTTAGCTGGTCCATCAGTTTTATTAGAAACTCATAA
Long Flanking Sequence:
TGATAAAGAGGAGCTGGTTGCTACTGATGTGAGTCAATGTTTGATTATTGATTTATTCTATATAGATATGACAGATCGTAGGTCTCATTCTTCTCTGTAATCTCCAGACTGCTATTGACATTCTGGGCTTCACTGGTGAAGAGAAAATGGGTATCTACAAGTTCACTGGAGCTGTGCTTCATCATGGTAACATGAAGTTCAAGCAGAAGCAGCGTGAGGAGCAGGCAGAGCCTGATGGCACAGAGGGTGAGACCCAGTTGCACTAATGTGTGTCATCACATATGATGCTTTTGACCGATCATTGTTTCTGTTTACAATAATCAATGGTTGAATTTAAAAGTCAGGAAAATAAATGATTGTATGGTAATTTTAAAATCACAGAGGCTGACAAAATCGCTTACCTTCTGGGTTTGAACTCTGCTGATATGCTGAAGGCTTTGTGCTACCCCCGAGTGAAGGTCGGAAATGAGTTTGTGACCAAAGGACAGACTGTGCCACAG[G/A]TATGCAGTAACATTTTTAGCTGGTCCATCAGTTTTATTAGAAACTCATAAGTGAATCAGAGTAGTTATTGCTAGTTGTTTAATTTTATTAAAGAGCATATTTTTAAAAAAATGAACTGTGTTCTACTTACAGGTGTACAACTCTGTTAGCGCCTTGTCCAAATCTATCTATGAGAGGATGTTCTTGTGGATGGTCATTCGTATCAACCAGATGTTGGACACAAAACAACAAAGAAATTTCTTCATTGGTGTGCTGGATATTGCTGGCTTTGAGATCTTTGATGTAGGAAGGATTCTTTCATTTCTTTATACTTCAAACTGAGACATATTCAGTAGTCAGTAAATAATCCTGTTTCTTCTCTAGTTCAACAGCATGGAGCAGCTGTGCATCAACTTCACTAATGAGAAACTGCAACAGTTTTTCAACCACCACATGTTTGTGCTGGAACAAGAGGAGTACAAGAAGGAGGGCATTGTTTGGGAGTTCATTGACTTCGGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6986
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051361 Essential Splice Site 631 1935 16 40
ENSDART00000124498 None None 452 None 14
ENSDART00000126873 Essential Splice Site 631 1935 17 41
ENSDART00000128949 Essential Splice Site 631 966 17 23
Genomic Location (Zv9):
Chromosome 5 (position 33848701)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31610933
GRCz11 5 32211086
KASP Assay ID:
554-4467.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTCTTTCTAGTTATTACATWATGTGTACCATTGTATWGTTATATAAAT[A/T]GAGACTGGTGGCGGAAAGAAGGGAGGCAAAAAGAAGGGTGGTTCCATGCA
Long Flanking Sequence:
TTTACTGGTTTATGGATATATTCATTTCCATTGTCTATTCTCAAAATCATACAATTTTTACTAACAAACTTACTAACCTTCTTTTACAAACAGCCCTTAGGTATCTTCTCCATCCTTGAAGAGGAGTGCATGTTCCCCAAGGCTACAGACACTTCCTTCAAGAACAAGCTGTATGATCAGCATCTTGGCAAGTGCAATGCTTTCCAGAAACCAAAGCCTGCCAAAGGCAAGGCTGAGGCTCACTTCTCCCTGGTCCACTATGCTGGAACTGTGGACTACAACATTTCTGGCTGGCTGGACAAGAACAAGGATCCACTGAACGAGTCTGTTGTGCAGCTTTACCAGAAGTCTTCTGTCAAACTGCTGGCTACTCTCTACCCACCTGTTGTTGAGGGTAAAGACATAAGTGTTAATATGTTCATTTGAATCATATTAACCAAACTTGGATTTTTTTCTTTCTAGTTATTACATTATGTGTACCATTGTATTGTTATATAAAT[A/T]GAGACTGGTGGCGGAAAGAAGGGAGGCAAAAAGAAGGGTGGTTCCATGCAGACTGTGTCTTCCCAGTTCAGGGTATGTTTTTGTTTGAGACCATTTTAAAACTGAAAACAGCTACATGGGTTTACCTAGTTGACTCTAGGTCAGAGAAACAATACATAAAAAATTGAATGAATATGAATAAAATACTTTTTATATGATTAAACAGGAAAACTTGGGCAAGCTCATGACCAACTTGAGGAGCACTCACCCTCACTTTGTGCGTTGTCTGATTCCTAACGAGTCCAAGACTCCAGGTAAAGAAATAAATGACTTACATATGTGCTGACATAAACACAATGTTAAATATTTTTGTTTACAATACTATCAATATTTACTAAGCTCATGATGTATACTTTTCCTTATAGGTCTTATGGAGAACTTCCTGGTTATCCACCAGCTGAGGTGTAACGGTGTACTGGAGGGTATCAGAATCTGCAGAAAGGGTTTCCCCAGCAGAATCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26506
Status:
Mutation detected in F1 DNA
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
ENSDART00000051361 Nonsense 884 1935 21 40
ENSDART00000124498 None None 452 None 14
ENSDART00000126873 Nonsense 884 1935 22 41
ENSDART00000128949 Nonsense 884 966 22 23
Genomic Location (Zv9):
Chromosome 5 (position 33849971)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31612203
GRCz11 5 32212356
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCTGAAGCCAAAAAGAAAGAGCTGGAAGAGAAGATGGTGGCACTGCTG[C/T]AAGAGAAAAATGATCTGCAGCTGGCAGTGGCTTCTGTGAGTATTCTTAAT
Long Flanking Sequence:
GTGATCAGTGTAGTTTAGATTAGACATCAATTTATTTTCCTTTTCTCTATTTACATGAATTCAGGTGTTCTTCAAAGCTGGTCTTCTGGGTACCCTTGAGGAGATGCGTGATGAGAAACTGGCAACTCTAGTCACAATGACCCAGGCTCTCTGCCGTGCTTACCTGATGAGGAGAGAGTTTGTGAAGATGATGGAGAGGAGGTGAGGGAAAAGCATGAGTTATAATTGTGTGAATGGTAAAAAGTAATGATTATGGCATTTAATGATGAACTATTCACAGGGAGTCCATTTACACCATCCAGTACAACATCCGCTCATTTATGAATGTCAAACACTGGCCATGGATGAAGGTTTACTACAAGATTAAGCCTCTGCTGAAGAGTGCTGAGACTGAGAAAGAGCTGGCAACCATGAAAGAGGACTTTGTCAAATGTAAAGAGGCTTTGGCCAAGGCTGAAGCCAAAAAGAAAGAGCTGGAAGAGAAGATGGTGGCACTGCTG[C/T]AAGAGAAAAATGATCTGCAGCTGGCAGTGGCTTCTGTGAGTATTCTTAATTTAATAAACTCAATCTCATCTCCATTAAAATTAGTTTGCAATGATATAACAATGTGTTTTCCTAACAGGAATCAGAGAATCTCTCAGATGCTGAAGAGAGGTGTGAGGGTCTGATCAAGAGCAAAATCCAGCTTGAGGCTAAACTCAAAGAGACAACTGAGAGACTGGAGGATGAGGAAGAAATCAATGCTGAACTGACAGCCAAGAAGAGGAAACTGGAGGACGAGTGCTCTGAGCTGAAGAAGGACATTGATGACCTGGAGCTCACCTTGGCTAAAGTGGAAAAGGAAAAACATGCCACTGAGAATAAGGTTGGAAGCTAAGGCTTTTTTACTTCCTTTTTAGAATTATTATTTAACTGTTGATAAAAGTATTCAATACAATGAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10296
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
Order Allele From EZRC
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051361 Essential Splice Site 1453 1935 30 40
ENSDART00000124498 None None 452 None 14
ENSDART00000126873 Essential Splice Site 1453 1935 31 41
ENSDART00000128949 None None 966 None 23
Genomic Location (Zv9):
Chromosome 5 (position 33852587)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31614819
GRCz11 5 32214972
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAATGCTTTGGCTGCCAACCTTGACAAAAAGCAGAGGAACTTTGACAAG[G/T]TAAAATATGGAATTAAACTGTGATTTGATTTTTCTCTTTAAGAAAGTAGT
Long Flanking Sequence:
CAATTTAATAGTATGTGACATGTTTCCTAGGCTAAGAACGCACTGGCCCACGCTGTACAATCAGCCCGTCATGACTGCGACCTGCTCCGTGAGCAGTTTGAGGAAGAGCAGGAGGCAAAGGCTGAGCTGCAGCGGGGAATGTCAAAGGCCAACAGTGAGGTTGCTCAGTGGAGAACCAAATATGAAACTGATGCCATCCAGCGCACAGAAGAACTTGAAGAGTCTAAGTAAGAACTTTACAATTGCAACTCATACTGTGAGTTTTTTTGTGTCATTGCATACATTTTTTTACTAATGACTATGAAATATTTAACAGGAAGAAGCTTGCTCAGCGTCTGCAAGAGGCAGAGGAACAAATTGAGGCAGTGAACTCCAAATGTGCATCTCTGGAGAAGACCAAACAGAGACTCCAGGGTGAAGTGGAGGACCTCATGATTGATGTGGAGAGAGCCAATGCTTTGGCTGCCAACCTTGACAAAAAGCAGAGGAACTTTGACAAG[G/T]TAAAATATGGAATTAAACTGTGATTTGATTTTTCTCTTTAAGAAAGTAGTATGAGCTTTCTTCTAGAGACTACAAGTTGAAAAACCTGATCGTAATATATTTCCCACTAAAGGTCCTGGCAGAATGGAAGCAGAAATATGAGGAAGGTCAGGCAGAGCTGGAAGGTGCCCAGAAAGAAGCTCGTTCACTCAGCACTGAGCTGTTCAAGATGAAGAACTCCTATGAGGAGACTCTGGATCAGCTGGAGACCCTCAAGAGAGAGAACAAGAATCTGCAGCGTAAGAATCAAACATTAAGAATAAAAATATGTGATGAATGAATGTTCTTTATGAAAGGATGATTTTTCTTTCTACAGAGGAGATTTCAGATCTGACAGAGCAATTAGGTGAGACTGGTAAGAGCATCCATGAGCTGGAAAAGGCCAAGAAGACAGTGGAGACTGAGAAGGCAGAGATTCAAACTGCCCTGGAAGAGGCTGAAGTGAGTATATGGAGATTTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40475
Status:
Mutation detected in F1 DNA
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
ENSDART00000051361 Nonsense 1918 1935 39 40
ENSDART00000124498 None None 452 None 14
ENSDART00000126873 Nonsense 1918 1935 40 41
ENSDART00000128949 None None 966 None 23
Genomic Location (Zv9):
Chromosome 5 (position 33854940)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 31617172
GRCz11 5 32217325
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGCATGAGCTGGAGGAGGCTGAGGAGCGTGCTGATATTGCTGAGTCC[C/T]AGGTCAACAAGCTCAGAGCCAAGAGCCGTGACGCTGGAAAGGTCAGTTGC
Long Flanking Sequence:
TTTATTATATATGTATTTAATTATTTTATTATCTATTTAGGTTCGTGAGCTTGAGAGTGAAGTTGAAGCAGAGCAGAGGCGTGGAGCTGATGCTGTTAAAGGCGTCCGCAAATATGAGAGAAGAGTCAAGGAGCTCACCTACCAGGTAAAGACATCTGAGTAAAAGTTTTAATCAAATATAAAATGAAGGTTGGTAAAATAGATCAAATTAATCTATGTTCCCTGTATGCAGACTGAGGAGGACAAGAAGAATGTCAACAGACTGCAGGATCTGGTTGATAAGCTTCAGCTGAAGGTCAAGGCTTACAAGAGACAGTCTGAAGAAGCTGTGAGTTCCTCTTTTGAGAACTTAGACACCTGTGAACTTTCAAGATGTTCTTTTACTGATACAGTTGTATGTGACTTTGCAGGAGGAACAAGCCAACTCTCACCTGTCCAAGTTGAGGAAGGTGCAGCATGAGCTGGAGGAGGCTGAGGAGCGTGCTGATATTGCTGAGTCC[C/T]AGGTCAACAAGCTCAGAGCCAAGAGCCGTGACGCTGGAAAGGTCAGTTGCATATTACAAGACTGTACTTTAAAATTAGTATTTAGCTTATGTTATGAATATATGGGGATTATTAACATGCCATATTTATGTGCTTCTTTTTTTCTAGGCCAAAGAAGAGTAAAGCCCTTAAACCTGAAGGAAGGCTCTACTGAAGTCATATAATATGACTGTTCTGTAGATATATTTTTAAATAAATATGTGCTTACTGGAAAATACATTTGTTATGGGTGATCTTTAAAATAACTTCACGCTAAAATGTATATTATTATGTATGTATGACAGCAACAGCTCCAGCAAAGGTAGAGTGATCGAATGAAGAGGGTTAGGGTTAGAAAAAAAATAACATTGCTTTATTTTACACTAGTGCTTTATTGAAGGAAGATTTCACTCAAAATGAATAGTTGCACACATTTATGAATGGATTGGGGTCCAAAAGTTGGTTCAATAGTGTATTTATAA
Associated Phenotype:
Not determined