Busch Lab

ZMP

myo1d

Ensembl ID:
ENSDARG00000036863
Human Orthologue:
MYO1D
Human Description:
myosin ID [Source:HGNC Symbol;Acc:7598]
Mouse Orthologue:
Myo1d
Mouse Description:
myosin ID Gene [Source:MGI Symbol;Acc:MGI:107728]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa35309 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa24915 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35308 Nonsense Mutation detected in F1 DNA Not yet available
sa42047 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38899 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa45464 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa35309
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
ENSDART00000067762 Essential Splice Site 188 1004 4 22
Genomic Location (Zv9):
Chromosome 12 (position 30052481)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 28389418
GRCz11 12 28504320
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAAGGAGACCCCATTGGCGGCCATATCAACAACTACCTGCTTGAGAAG[G/A]TAGGGGGCGCTTAATTACTTCCTTTAAAATTATATTTAAAAGAATACAAC
Long Flanking Sequence:
TAGGTCATGCATGGCTGTTCGGCAAGAGAACCAATGCTGAGCTTTCTGTGGTCTGACCCGTGCAGCAGGACCCATAAATCATCCCCTGAAATGTTTTAAACCACCATACCGGCATACCACATGGTGATACTCTATACGCTAATATGGCCAGATATAACCATGTATAATGGCTCATAAATGCTTCATACAGACATGTTTGTGTATTTACTGTAAAATCAAATGTTGGGAGCAATCAGATCATATTGAAACTGACATTGATTTAGCTCTAGAGGTAAAGTGATGCACACTAGGCTAATAAATGCTGTCGAAGTGAAAAGAGTGTGTGTTTATACAGGGTGAAAAACATGCTGCTGAAGTCCAACTGTGTCCTCGAGGCTTTTGGAAATGCCAAGACCAACCGCAATGATAACTCCAGCCGGTTCGGCAAGTACATGGACATCAACTTTGATTTTAAAGGAGACCCCATTGGCGGCCATATCAACAACTACCTGCTTGAGAAG[G/A]TAGGGGGCGCTTAATTACTTCCTTTAAAATTATATTTAAAAGAATACAACAAAAATAAAGATCAGTTACAAATGCACTGCAAACCTGGAGCAATTACTATTAGTCCAAGCTTGATTTGTCATTATCCATTGGCTACATTTGCCATTGTAATGTTATTAGAATGGGATTTTTGCAGCATTGCAATTAAATTTTACCTCTTGTAAACGATGCTTTTGCTAAGCTCACAGTAACAATAATGGCAAGTGCCGATCCCTTTATGTGGCAATTGCTGTGTTGTGTGCTCCAGTTTTATTTGCAATAAACAAGCACATTAAAACCTTAATTGCTTTATTATCATTGTGACCAAAGTGCACATGTTTTGTTCTCACCACTTTTAAATGAACTGCAAATTTTCCTTAACTCTGAATTGCTAAATTAAAACAGTGGACACTATTTTGCTCAAAATTTAGAATAATAAGTTGTTGTAATAATTACATTAATTAACAACTTAAAAAAATTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24915
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
ENSDART00000067762 Essential Splice Site 394 1004 9 22
Genomic Location (Zv9):
Chromosome 12 (position 30044714)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 28381651
GRCz11 12 28496553
KASP Assay ID:
554-7619.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCATTGGAGTTCTGGACATCTATGGCTTTGAGATCTTTCAGAATAACAG[G/A]TAAGAGCATAATACTGTACCATAGAGATATTTTGTCTCTGTGCATAATCA
Long Flanking Sequence:
AGCCTGGTGAGACTTTTCTTAAAAGCAATAAAATATTTTTCCCTGACCCATTGTTTGAACAGTAGCAGCTTTATTTTTTTATAACTTTATAAGATGTAAATATATGTTTCAATTGCTGTTTATTTTATCTATACATTTCAAAAAACACTTTTCTTACTTAGTTTTTTTGTCTTTCTAGTCCAAATATCTAAAATAACTTAAATAAATAAGCATTTTCTAGACAACAGAAAAGTTTTGTTTTAAGAATCAATATGCCAAAATTAAGTGAGTTTTTCCTTAAAACAAACAAAATTATCTGTCAATAGGTAAAGAGAAGATTTGACGAATCAACCATTTTTTATGTGTTACTTACAGGCCATCTATGAGCGCCTTTTCTGCTGGATTGTGGGACGAATCAATGACATCATTGAGGTGAAAAACTACGACGCTCGAGTTCATGGTAAGAACACAGTCATTGGAGTTCTGGACATCTATGGCTTTGAGATCTTTCAGAATAACAG[G/A]TAAGAGCATAATACTGTACCATAGAGATATTTTGTCTCTGTGCATAATCACAAATGCAGCATCTCTCCAACATCTTCTTTGTTTTCTCTAGCTTTGAGCAGTTCTGTATAAATTACTGTAATGAGAAACTGCAGCAGCTCTTCATTCAGCTGGTGCTAAAACAAGAGCAGGAAGAATACCAGCGAGAAGGCATCCCTTGGAAACATGTGGGTTTTATTCAACTGTTTCTCTAGAAGCTTTTTACGTCTTTATTATTTTATATTATACTTCAAAAAACTTGTTTTACATGGGTCTGCCTGGCTTTATTGCAGTTTGCAAATGAGCTTTGTGTTTGTGTGTTCATGGAAACAGATTGACTACTTCAACAATCAGATCATCGTAGATCTCGTGGAACAGCAGCATAAGGGCATTTTTGCAGTGCTGGATGAAGCATGCATGAATGTGGGGAAGGTGACGGATGAGATGTTCCTACAGGCCCTCAATGGGAAACTGGCCAAACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35308
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
ENSDART00000067762 Nonsense 447 1004 11 22
Genomic Location (Zv9):
Chromosome 12 (position 30044320)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 28381257
GRCz11 12 28496159
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAACAGATTGACTACTTCAACAATCAGATCATCGTAGATCTCGTGGAA[C/T]AGCAGCATAAGGGCATTTTTGCAGTGCTGGATGAAGCATGCATGAATGTG
Long Flanking Sequence:
TCAATGACATCATTGAGGTGAAAAACTACGACGCTCGAGTTCATGGTAAGAACACAGTCATTGGAGTTCTGGACATCTATGGCTTTGAGATCTTTCAGAATAACAGGTAAGAGCATAATACTGTACCATAGAGATATTTTGTCTCTGTGCATAATCACAAATGCAGCATCTCTCCAACATCTTCTTTGTTTTCTCTAGCTTTGAGCAGTTCTGTATAAATTACTGTAATGAGAAACTGCAGCAGCTCTTCATTCAGCTGGTGCTAAAACAAGAGCAGGAAGAATACCAGCGAGAAGGCATCCCTTGGAAACATGTGGGTTTTATTCAACTGTTTCTCTAGAAGCTTTTTACGTCTTTATTATTTTATATTATACTTCAAAAAACTTGTTTTACATGGGTCTGCCTGGCTTTATTGCAGTTTGCAAATGAGCTTTGTGTTTGTGTGTTCATGGAAACAGATTGACTACTTCAACAATCAGATCATCGTAGATCTCGTGGAA[C/T]AGCAGCATAAGGGCATTTTTGCAGTGCTGGATGAAGCATGCATGAATGTGGGGAAGGTGACGGATGAGATGTTCCTACAGGCCCTCAATGGGAAACTGGCCAAACATGCCCACTACACTAGCCGCAAGGTACAGAACTGCTTTAAAGCTCTTTATTGTGTCATAAAGGTTTTTGTTAGTATTTGTGAAAGGTGTCTTTTATGCTTACCAGGGATGCTTGCAAAATACAGTGTAAAAAGAATGTGATATTTTATAATAATTTCAAAAACATTTTAACATAAAATAATAATAAACAAAATATTATATACAGTCAGGTCCATAAATATTGGGACATCTACACAATTCTAACATTTTTGGGTCTATACACCAACACAATGGATTTGAAACAAAAGAAGACTCAGCTTTAATTGGAAGGTATTTACATTCAAATCAGGTGAACAGTGTAGGAATTACAACTGTTTGCATATGTGCCTCCCACTTGTTTAGGGACCAAAAGTAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42047
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
ENSDART00000067762 Essential Splice Site 538 1004 13 22
Genomic Location (Zv9):
Chromosome 12 (position 30026315)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 28363252
GRCz11 12 28478154
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAACAAGGACACCTTATTTCAGGACTTCAAGAGGTTACTTTACAACAG[G/A]TCTGTATTATCATACAATAATACAGTGCCTCCATTCTTATTTACATACCT
Long Flanking Sequence:
AAGGTGAAGTGTGTTCTTTTTGATGGTAAAGTAATGTATTCAGTTCAAGCCAGCTGTAAGTTAGCTATTTGTAGTTTCATTACCTTGAGAAATATAAATGCAGTCTTTGTGCACTGACAAAGCGTACTCGATTTCTATGAGCTTTTCAGCCAGACCAGCAACAGCATCATGAAACTCCATTCATTTTCCCCAAAGGGAAATGGATTTTTTGAAATAGCTACTAAACCTTTGTAGACTGCCCTGTTGCAAGCTCTGATGTTGTTAATTGATTGTATATGCTTTAGTTGGACCCACTCATTTGCATTAATTCAGCTTATTTTTTAAAAAAATATGTGTTTAATAATTCACTAGCCTTTAAAGAGTTTGCCATTTTCAAATTATATACCTGCTTGTCTATTATAGTCAATGTGGTTGTTTCATTTCAGTTACTCCGTTGTGGGCTTCATTGACAAGAACAAGGACACCTTATTTCAGGACTTCAAGAGGTTACTTTACAACAG[G/A]TCTGTATTATCATACAATAATACAGTGCCTCCATTCTTATTTACATACCTGCCATACCTACATAACTTTTATGTTTCACAGCTCAAACCCTGTGCTTAAGGCCATGTGGCCGGAGGGCAAGCTGAGCATTACAGAGGTCACCAAACGCCCCCTGACTGCTGCCACGCTGTTCAAAAACTCCATGATATCTCTGGTGGAGAAGCTGGCCAGCAAGGCAAGTTTATTTGAAAAAGTTTTGTGTATACTATGATTAGTGTCAGACGGTATCTGTGGACATTTTTTGCTATTTCTGCTGAAAATTTTGTAAAAAATCTGCAGATTTCTGCTGAAGGGTTTTAGGATTATCATAACTAAAAACTTAATATATGAAATAAAAACTAATAAATTTGTAACTTTTATTTAATGTTTACAATGCATATCCAATTAGATCTACTTATTTGGTAAATAAAGCAAGTCTCTTATAATATATCTACTAAAAGACAGAAAATATTACTTTTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38899
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000067762 Essential Splice Site 582 1004 14 22
Genomic Location (Zv9):
Chromosome 12 (position 30026099)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 28363036
GRCz11 12 28477938
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGTTCAAAAACTCCATGATATCTCTGGTGGAGAAGCTGGCCAGCAAGG[C/T]AAGTTTATTTGAAAAAGTTTTGTGTATACTATGATTAGTGTCAGACGGTA
Long Flanking Sequence:
GCTACTAAACCTTTGTAGACTGCCCTGTTGCAAGCTCTGATGTTGTTAATTGATTGTATATGCTTTAGTTGGACCCACTCATTTGCATTAATTCAGCTTATTTTTTAAAAAAATATGTGTTTAATAATTCACTAGCCTTTAAAGAGTTTGCCATTTTCAAATTATATACCTGCTTGTCTATTATAGTCAATGTGGTTGTTTCATTTCAGTTACTCCGTTGTGGGCTTCATTGACAAGAACAAGGACACCTTATTTCAGGACTTCAAGAGGTTACTTTACAACAGGTCTGTATTATCATACAATAATACAGTGCCTCCATTCTTATTTACATACCTGCCATACCTACATAACTTTTATGTTTCACAGCTCAAACCCTGTGCTTAAGGCCATGTGGCCGGAGGGCAAGCTGAGCATTACAGAGGTCACCAAACGCCCCCTGACTGCTGCCACGCTGTTCAAAAACTCCATGATATCTCTGGTGGAGAAGCTGGCCAGCAAGG[C/T]AAGTTTATTTGAAAAAGTTTTGTGTATACTATGATTAGTGTCAGACGGTATCTGTGGACATTTTTTGCTATTTCTGCTGAAAATTTTGTAAAAAATCTGCAGATTTCTGCTGAAGGGTTTTAGGATTATCATAACTAAAAACTTAATATATGAAATAAAAACTAATAAATTTGTAACTTTTATTTAATGTTTACAATGCATATCCAATTAGATCTACTTATTTGGTAAATAAAGCAAGTCTCTTATAATATATCTACTAAAAGACAGAAAATATTACTTTTCAAACTGTATTGTTAATAAATCAAATTAACATTTTAATATTACTATTATTATTTTACAATAATGTTTGAATAAATATACCTTTACACAAATTTACACTAGTAAATACATAGATTCAAAGATGGGCTAAAAATCTAAAGAAATCTGCAGATTTCTGTGCGTGCAGATTCTGTGTGGGCCTAACTATGATCTTGTTTGTTTTGCATTAAAAGGCTACATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45464
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
ENSDART00000067762 Nonsense 738 1004 17 22
Genomic Location (Zv9):
Chromosome 12 (position 30007553)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 28344490
GRCz11 12 28459392
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGTGCCGCGCTCATCATTATCCGGGCATACAGACGATACAAGGTGAAGT[C/A]GTACATCCGTGAGGTTATCCGACGCTTCAAAAACGTCCGCGACATGAAGG
Long Flanking Sequence:
TTTGGTTAAGGAGACATGGAAAATGTGATGAACGTGGTTGAGAAACACAGGTTCAAATAATTTTTCAGTAAAATAGCATTTACATTTGTGTAAAAAAAGGAATAGTAACTAAAGCAAAAGTTGCTGAAATGTAGATTTTGATTGTCTTTCATCTAAAACTTTACAATTCTTGAGTTTTATTGGGGACAATGTAAATGTTTTATGTTCAGTTCACTTAAGTTTGTAAAAACAATTAAGTTTACTTATTCGGTTTGTGGTGGGACAATGTGAAGGAATTGTGTGGAACATTTTTTTTTACAGTGTTCCATGTGTCTCAACTAACACAGTATTATAATTATCTGCATATTGTAAAATTTTAATTACTCAGCAATTTTAATCTCGCTCTTTCTCCTCTCACTGTGTGTTTCAGGTTTGGCGTGGTACTCTGGCCAGAATGCGTTACCGCCGCATGCGTGCCGCGCTCATCATTATCCGGGCATACAGACGATACAAGGTGAAGT[C/A]GTACATCCGTGAGGTTATCCGACGCTTCAAAAACGTCCGCGACATGAAGGACCACGGAAAACATGTGAAGTGGCCCACACCCCCTAAAGTCTTGCGCAAGTTTGAGGAGGCACTGAGGAGCATCTATAACAGGTGGGCATCTATGATGGTGGGTAGACTCTATGTGACTCATGGAACAGTCATATATGAGTCCAGATGTGCCCGGTGTAAAAGTAATAAAGTGAAATGTCTCTGACTCAATGCATCACTTTCAAGGCTTTATCATTGTTAGACAAGGAATTTTTTTTTTTTTGCTGTAGGCTTTTGTGTTTCATTGGTGTTTAAGCACAGAACAGAAAGGCTGTCTTGTGTTTCACTGGGCTGTTGTGCCCGGAGCACATATTGATCTTTGGATCAAAGTCTTGTTGGAGATCTGTTCACAATAGCCTTAACACGTCTCTGACCTCGAGAAAACAATAGAGAAAAACAACTTGTTAAAAAGTCCAACTGTGTCCAACATT
Associated Phenotype:
Not determined