Busch Lab

ZMP

myo6a

Ensembl ID:
ENSDARG00000044016
ZFIN ID:
ZDB-GENE-040819-2
Description:
myosin VIa [Source:RefSeq peptide;Acc:NP_001004111]
Human Orthologue:
MYO6
Human Description:
myosin VI [Source:HGNC Symbol;Acc:7605]
Mouse Orthologue:
Myo6
Mouse Description:
myosin VI Gene [Source:MGI Symbol;Acc:MGI:104785]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa23617 Essential Splice Site Available for shipment Available now
sa3048 Essential Splice Site Available for shipment Available now
sa43364 Nonsense Mutation detected in F1 DNA Not yet available
sa16041 Nonsense Available for shipment Available now
sa6610 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa23617
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000015558 Essential Splice Site 516 1253 14 31
ENSDART00000064620 Essential Splice Site 516 1292 14 35
ENSDART00000135066 Essential Splice Site 516 1288 14 34
ENSDART00000136768 Essential Splice Site 516 1253 15 32
Genomic Location (Zv9):
Chromosome 20 (position 778943)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 734808
GRCz11 20 755634
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCTGGGAGTCAATGAAGTGCACTACGTTGATAATCAGGACTGTATAGG[T/G]CTGTATCTCAGATAAAACTCTGACTTGATTGAGCTGTTGAAATGATATCT
Long Flanking Sequence:
TCAAAATGTTTCCAATTATGATTTCGATTAATGGTTCAGTCCTAGATTATCAAAATGTTTCCAATTATGATTTTGATTAATGGTTCAGTCCTAGATTATCAAAATGTTTCCAATTATGATTTCGATTAATGGTTTAGCCCTAGATTATCCCAATGTTGTGAATCACGATATCTATTAATGGATTAGTTCTAGATTATTGCAATGTTTCAAATCATGATTTCCATTATTGGTTCAGCCCTAGATTATTCCATTAATGGTTCAGCTCTAGATTATCGCAGTGTTTCGAATCATGATTTCAATTAATGGTTCAACTCTAGATTATCGCAATGTTTTAAATCAATTTTCAGCTCTACACTGAATCAAAATGAGCTATTATATGTGATGCACTGGTCTGATACTCTGGCTTTTGTTGTGTACGTTTAACAGGAGCAGGAACTGTATCAGAAAGAAGGCCTGGGAGTCAATGAAGTGCACTACGTTGATAATCAGGACTGTATAGG[T/G]CTGTATCTCAGATAAAACTCTGACTTGATTGAGCTGTTGAAATGATATCTGTATTATATCTACCCCTTTTATCTTCTTTGGTTCAGACTTGGTGGAGTCGAAGGTAGTAGGCATCTTGGACATCCTGGATGAAGAAAACCGACTACCTCAACCCAGCGACCAGCACTTTACTGAAACCGTCCACAGCAAACACAAGGACCATTTCCGGCTGACTGTGAGTCTCGCTTCATTTCAGCTCGTTTTGCTGTAGTTTAGGGGCTTCGGATTTAATTAATTATTAATTAACTATATTTTAGTATAATTTTGTTCTGTGCTGGGTTGCGGCTTGAAGGGGATCCGCTGCTTAAAACATATACTGGAATAGTTGGCGGTTCATTCCACTGTGGCGACTTCTTAAATGGAGACTAAGCCGAAGGAAAACGAATGAATGAATGTGTTAGGGGTATTTTGAAGTGTCCGCTATATCAATATTGTGCATGTTCATTATCACGATATGTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa3048
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000015558 Essential Splice Site 761 1253 21 31
ENSDART00000064620 Essential Splice Site 761 1292 21 35
ENSDART00000135066 Essential Splice Site 761 1288 21 34
ENSDART00000136768 Essential Splice Site 761 1253 22 32
Genomic Location (Zv9):
Chromosome 20 (position 782077)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 737942
GRCz11 20 758768
KASP Assay ID:
554-2521.1 (used for ordering genotyping assays)
KASP Sequence:
AAACGATTATAAATTTGGCTTGACAAAAGTGTTCTTCAGACCTGGAAAGG[T/A]AATGTGACTCGAGTTTTAYGGTTGTTTTTAATTTNNNNNNNNNNGTGGTG
Long Flanking Sequence:
GCCTGATGTATCGGTACGAGATACTCGGCTGCAAAAACAAAAAATCTATTAAAAGTAAAGTATTATTATTATTATTATTGTCACATCATGGGTTTTTCAGGTTTACAATCGAAGGTTGCAAATGATTTGATGCCAAGATGCAGACAATCAGTTCAGTGTGTTGATTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGGTTCAGGGATGGTGTCTGTACTGGATCTGATGCAGGGTGGTTTCCCCTCACGAGCGCCTTTCCATGAGCTCTACAACATGTACAAACAGTACATGCCGGCTAAACTGACACGACTGGACCCCAGACTCTTCTGTAAGGTGTGTGTGTAAATACAGTACACCAGCAAGATGTCATATCATAGCATTCAGTAAAGTCATTTAACGTTTGTGTCTTTCCTCCTCCACAGGCGTTGTTCAAAGCTCTCGGGCTGAATGAAAACGATTATAAATTTGGCTTGACAAAAGTGTTCTTCAGACCTGGAAAGG[T/A]AATGTGACTCGAGTTTTATGGTTGTTTTTAATTTGCCGTTTTCAGTGGTGATATTGTGAAATTGATAGTCAATGCTTCAATGATTCTCTTAATTCGGAACTCGTGATGCACGCGATGTTGGTTGGTTTTGTTGTTGGTTATGTCTCACACACAAACGTTTTAGTTTGTTTAGCAATGGTAATGCTAGAAGTCAGTGTATTGCCGAAGGATGCATTCCTCTCAGATTGTCGGTTGGTTTGTATCGTGGTTCCTGTTATCATGGTTCTCAGTTTGATTCCGTTTACACTGTCAGAAATATACCTTGCCATAATTTCTCCTAGGGGTGTCACGATTTCGATTTTTAATCGAAATCGATCGAAATTTATGCTCAATTTCGATTATCGAATCAAAAAATAGAATCGTCGATGTTGCCACGCCCCCATGTCACGTCAGCTTGGCTTGCCAAGCAGGAAAATAACGGGCTTGTTGAAGTGCTTGTTAAACTGCAGAAGCAGGAGACC
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461

Mutation Details

Allele Name:
sa43364
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000015558 Nonsense 961 1253 26 31
ENSDART00000064620 Nonsense 961 1292 26 35
ENSDART00000135066 Nonsense 961 1288 26 34
ENSDART00000136768 Nonsense 961 1253 27 32
Genomic Location (Zv9):
Chromosome 20 (position 789585)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 745450
GRCz11 20 766276
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTCATGCAGTTCTACTTCTGTTTGTTGTAGGAAAGCCGAGATGGAGT[T/A]GAAGAGGAAGCAGGAGGAAGAAGAACGCAAGAAAAGAGAGGAGGAAGAGA
Long Flanking Sequence:
CTGCGTAAGGTGTGTTTGATTAGGGTTGGAGCTAAACTTTCCAGGACAGCGGACCTCCAGGACTGAGTGTGGACACCCCTGCATTAAAGTCTATGCTACCGCTCATACAGTATCAGGGGTTCTCAATCTTGGTTTTGGAGGGCCGGTGTCCTGCTGATTTTAGCTCCAACCCCAATCAGACACACCTGGGCTAGCTGATCAAGCTCTTACTAGGCTTTCTAGAAACATCCTTGCAGGTGTGTTGAGGCAAGTTTGAGCTAAACGTCCAGGACTGAGTTTGAGAACCTCTGCCTTGTAGAAACCCTGTCATCAGTTTCCTGAACAGAAGCATTATAGTGACTGAAGCCTTGTGTATTTCTGATCTAGATCTTATTGCAAACTCTTCATCCGTGTGTGTATTTTATTTATTCTCGTTACGTTTGGTTCGACCTTGTAGTTGATCATCAGAATTTCTTCATGCAGTTCTACTTCTGTTTGTTGTAGGAAAGCCGAGATGGAGT[T/A]GAAGAGGAAGCAGGAGGAAGAAGAACGCAAGAAAAGAGAGGAGGAAGAGAGGAAGCTGCAGGTGACTTGGTTCTTCTGCTTTTCTTCCGTCTTAGCCACAGTGAACTTTTTGGTTTGGGCTTTTGTTCTCATGACCAGAGCTACTGCTGCCACGTCTTGGTGGTGCTCATGGTTTTTTAACGCAACTGATAGAGAGCTTCAGGAATGATGTCTTTATAGGCCCGTGCTTCAGTTAAAACCATTAACTTCACCAACACTGAGGGTGCTTTCACACCTGCCTTATTTATAAGTTCGATTGAATCGCACTAGAGTTTGTTTCCCCTGTTGGTGCGGTTCGTTTGGGCAGGTGAGAATGCAGCAATCGTACTCGAGTGCGCACCAAAAGCGAACCAAATAAGCGTACCGAGACCTGCTTGAAGAGGTGCTCTCGGTACGCTTTCAAACGAACCCTGGAGCGGTTCGTTTGTGGGGAGAATATGATCCGTACTAAAACAGGTCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16041
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000015558 Nonsense 1135 1253 30 31
ENSDART00000064620 Nonsense 1170 1292 33 35
ENSDART00000135066 Nonsense 1170 1288 33 34
ENSDART00000136768 Nonsense 1135 1253 31 32
Genomic Location (Zv9):
Chromosome 20 (position 798761)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 754626
GRCz11 20 775452
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGTGGTGCCRGCTGCAGTGCCCCGYCAGCATGAGATCGTCATGAACCGA[C/T]AGCAGCGCTTCTTCCGCATCCCCTTCATCCGGCCYGGAGACCAGTACAAA
Long Flanking Sequence:
TATAGACATTATAGTGGTGTTTAGACATTATAGAAGCCTGTTTTATAGACATTATAGAGGTGTTTATAGACATTATAGAGGTGTTTAGACATTATAGAAGCCTGTTTATAGACATTATAGAGGTGTTTATAGACATTATAGAGGTGTTTATACATTATAGAAGCCTGTTTATAGACATTATAGAGGTGTTTATACACATTATAGAGGTTGTTAGACATTATAGAGGTGTTTAGACATTATAGAAGCCTGTTTATAGACATTATAGTGGTGTTTATAGATATTACATGTTTAATTATAGACATTATAGAAATGTCTGTATATACATTATAGAATTGTGTTTATAGACATGATAGAAAGTGCTTGACTCTGCTGTTGATGAATGAGCATGAGCCCTGTCGAACAGTGTTCAGTAAAGCCTTGTGTTTGCTCGTCCTGCAGCCCAGCAGAACCCGGTGGTGCCGGCTGCAGTGCCCCGTCAGCATGAGATCGTCATGAACCGA[C/T]AGCAGCGCTTCTTCCGCATCCCCTTCATCCGGCCCGGAGACCAGTACAAAGACCCTCAGAGCAAGAAGAAGGGCTGGTGGTACGCGCACTTCGATGGGCCGTGGATTGCCCGACAGATGGAGCTGCACCCTGACAAACACCCCATTCTGCTGGTGGCAGGTCTGCGTCATCTTCAAAGCCTTTCTTACTCAGCATAAGTCATAGTTGGTAAAGGTAGAGCGCAGTGCATGCAGAGTAGCACACACACATCTTATGCATTCCTGTTTATAGAGGAAATATAGAAATAGCACACACACACACTTCATCAGATAACTGTGTGTAAAATGGAGGTTCTGTGAGGCTGAATCTGCATCACTCTGAGAAACACACTCACTGATATCTCGTCCCTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAGGTAAAGATGATATGGAGATGTGTGAGTTGAGTCTGGAGGAGACGGGTCTGACCCGGAAGCGAGGCGCTGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6610
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000015558 Nonsense 1243 1253 31 31
ENSDART00000064620 Nonsense 1278 1292 34 35
ENSDART00000135066 Nonsense 1278 1288 34 34
ENSDART00000136768 Nonsense 1243 1253 32 32
Genomic Location (Zv9):
Chromosome 20 (position 799357)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 755222
GRCz11 20 776048
KASP Assay ID:
554-4737.1 (used for ordering genotyping assays)
KASP Sequence:
ATCCAGTACCTGAGGAACGCCATCGAGAGCAGACAGGCCAGACCCACATA[C/A]GCCACCGCCATGCTGCAGAGCATGCTCAAATAAACACACACACACACACNNNNNNNNNNT
Long Flanking Sequence:
GGGCCGTGGATTGCCCGACAGATGGAGCTGCACCCTGACAAACACCCCATTCTGCTGGTGGCAGGTCTGCGTCATCTTCAAAGCCTTTCTTACTCAGCATAAGTCATAGTTGGTAAAGGTAGAGCGCAGTGCATGCAGAGTAGCACACACACATCTTATGCATTCCTGTTTATAGAGGAAATATAGAAATAGCACACACACACACTTCATCAGATAACTGTGTGTAAAATGGAGGTTCTGTGAGGCTGAATCTGCATCACTCTGAGAAACACACTCACTGATATCTCGTCCCTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAGGTAAAGATGATATGGAGATGTGTGAGTTGAGTCTGGAGGAGACGGGTCTGACCCGGAAGCGAGGCGCTGAGATTCTGCCGCGTCAGTTTGAGGAGATCTGGGAGCGCTGCGGGGGAATCCAGTACCTGAGGAACGCCATCGAGAGCAGACAGGCCAGACCCACATA[C/A]GCCACCGCCATGCTGCAGAGCATGCTCAAATAAACACACACACACACACTGAGAGAGATGCGCTCACAGAGACACACACACAGAGAGACACGCTCTTACATTCACAATCACACACACACAGTCTCACACACTTTCTTCCTCACAACAGACACACACATTCACAAAAACACACACACGCACTCTCTCATACACTTTCTCTCTCTCTCTCTCACACACACACACACTCTCTCTCTCAATCACAGACACATACACACACACATATACCCATACACTTTCACACACATACACAGACACAAATTTTCTCACATACACTCACTCACACACACCGACACGCTGTCTCACAGATACACACACACACATATGCTTACTCCCACACTCTTACACACACAAACACATGCATACAAACACACACACACTCACACCCACACTATATCTGTCACACATATGTACACGCACACACATGTACACACACACACACACACACACACTCTCTCACACAT
Associated Phenotype:
Not determined