ZMP
myo1c
Ensembl ID:
ZFIN ID:
Human Orthologue:
MYO1C
Human Description:
myosin IC [Source:HGNC Symbol;Acc:7597]
Mouse Orthologue:
Myo1c
Mouse Description:
myosin IC Gene [Source:MGI Symbol;Acc:MGI:106612]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35902 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16637 | Nonsense | Available for shipment | Available now |
sa22660 | Nonsense | Available for shipment | Available now |
sa7408 | Missense | Mutation detected in F1 DNA | Not yet available |
sa12270 | Nonsense | Available for shipment | Available now |
sa44824 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35902
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087926 | Essential Splice Site | 149 | 1028 | 4 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 27676025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 28394265 |
GRCz11 | 15 | 28327141 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTCTGAATTGTTCTATTCATCTATATTCCATCATTGTTTGTTTTCTCA[G/A]GCCTTTGGAAATGCAAAAACTTTAAGAAATGACAATTCCAGTCGCTTTGG
Long Flanking Sequence:
TGCCAGTGATCACGTGCAGACTGTCAAAGATCGCTTGCTACAATCCAACCCTGTGCTGGAGGTACACATGCACTCAGCACTTCTAATCCAATGATTTTCATGGCATACAATTTTACTAATCCCCAAGTGCCAGCATGTAGTGGAGAGATCAGCACAGGCTGTAATTCCTGCCCTGGGCTGCTGTCATTGCACAAAATACTCCAAATGACTCCCAGCGATGCCAAGGAAAAGAGCAGAGTTTATTCTGAGAAGCCGGTAGTCCCGCTAAACCTCTCCAGTAATTATATGCCACAGTTACTATCTGTACGATAAGATTGGAACATACATGAAGACGTCTAAAAATGGGATAGGCCAAAGGAAGTGGCGCAGACGGCCAGTTTTACCAGATGTTTTGCAGATGTGCTGGAAACTGGCAGTGTGTGCACATCTAGAGTGTCTTTTTTTCTCTGCCATTCTGAATTGTTCTATTCATCTATATTCCATCATTGTTTGTTTTCTCA[G/A]GCCTTTGGAAATGCAAAAACTTTAAGAAATGACAATTCCAGTCGCTTTGGGAAATACATGGACATTCAGTTTGACTTCAAGGTGAGGTTACTCATGTTTAAAAGGTTATTTCACATATTTGCTGGTAATTTACTCCCCTCAGGTGATCTTAAGCTTTTTTAATGGTCAGTACAGTATGATTCGGCTTAGCATTGCTTCAGTTTGGTTTCGCCCAACAATACAACAGTGGCCTGCCGATGACTTTTTCAATATAGCAGGTTTGGTGTCTTTTGTGGTAGTGATGATTCTCTCTGACCACATTTTGGTAATGAACTGTTTGCTATTGTTGGCATCCAGCATTCTTTTTCCTGCAGTCACTGATCCACAAAACTAAAGCCAACTCAATCCTTAAGGCATCCAGACAGTGGATGCCCTGCACACATGACAGTTGGAAGTACACACTGGATGTGCACATTCGCACCACATTCTGACTGGGCACCACAGACGCCACTGATGTACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16637
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 |
---|---|---|---|---|---|
ENSDART00000087926 | Nonsense | 229 | 1028 | 5 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 27678334)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 28396574 |
GRCz11 | 15 | 28329450 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGAGAGGAYGATCTGCTTAGGAGACTAGGYCTGGAGAGAAAYGCCCAA[C/T]AGTACCAGTATCTGGTCAAGGTGAGAGACTGACCTCGCTTGATATGATAC
Long Flanking Sequence:
ATGACTAAAATAATTTGACAGTAACGTTCAGAATCACTTCTTTCTTTGGGAGAACAAGAAAATTTATTGTGCTCTTTTACATTCACAATCAGTTATTTTAACACTGCAATACAAAAGCATTATTGTTGTTATCAACTGAAACTTACATCTCAACTGCTGTGATCCACTTTCTGTCGATGCACCTTTACCCCTACAATGCTCTTCTTGGTTTGGGGATTTGCCTGCATCTGCTTGTGTGTTCTTGTTCTTGTGCTTGTGTGTTGAATTATTCGTGCTTGCATGCGTGTCAGAAACCCGGTATTATCCCCTCTGCTTCTCCCTTTGGGTGTCCCCGTTGGCAGGGTGCTCCAGTCGGCGGTCACATCCTGAACTACCTGCTAGAGAAATCCCGCGTCGTGCACCAAAGCAACGGCGAGAGGAACTTCCATATCTTTTATCAGCTCATCGAAGGAGGAGAGGACGATCTGCTTAGGAGACTAGGCCTGGAGAGAAACGCCCAA[C/T]AGTACCAGTATCTGGTCAAGGTGAGAGACTGACCTCGCTTGATATGATACAGCAGATGTCTATAGAGAAACCAAAACTGGCTTAAAAAAAAAGCTGGGGTTTTGTAGCCATTTCACATGCTTCAGATTCAACTCATTTCCTGCAAAAAATACTTTTATAAAACAAGTATAAAAAAAAAGTGTAAATAAAAAAGTATAAATACTTTTACAAAAAATAGAGTTTTGCTTACCTCAAAATAATCTACCACTGGGGTAAGCAAAATAACTTCTTTAAAAAACATTGACAACTTCTTTATTTATATAGTACATGCATTAAAACATTATAAATATATGTTGAACAAGATAAATAAAACAGATTTGAATTCAAATTTCAGCAAACAAACACCCTTTATTCGTTTATTCCTTTATTAAGATGTTCATGGTAATGTTTACTTTCACCGTTTCATTTAGGGAAACTCCTGAAATAAATATGTTATATCTCTGAACTTTATTAATAAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22660
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087926 | Nonsense | 232 | 1028 | 5 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 27678345)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 28396585 |
GRCz11 | 15 | 28329461 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCTGCTTAGGAGACTAGGCCTGGAGAGAAACGCCCAACAGTACCAGTA[T/A]CTGGTCAAGGTGAGAGACTGACCTCGCTTGATATGATACAGCAGATGTCT
Long Flanking Sequence:
AATTTGACAGTAACGTTCAGAATCACTTCTTTCTTTGGGAGAACAAGAAAATTTATTGTGCTCTTTTACATTCACAATCAGTTATTTTAACACTGCAATACAAAAGCATTATTGTTGTTATCAACTGAAACTTACATCTCAACTGCTGTGATCCACTTTCTGTCGATGCACCTTTACCCCTACAATGCTCTTCTTGGTTTGGGGATTTGCCTGCATCTGCTTGTGTGTTCTTGTTCTTGTGCTTGTGTGTTGAATTATTCGTGCTTGCATGCGTGTCAGAAACCCGGTATTATCCCCTCTGCTTCTCCCTTTGGGTGTCCCCGTTGGCAGGGTGCTCCAGTCGGCGGTCACATCCTGAACTACCTGCTAGAGAAATCCCGCGTCGTGCACCAAAGCAACGGCGAGAGGAACTTCCATATCTTTTATCAGCTCATCGAAGGAGGAGAGGACGATCTGCTTAGGAGACTAGGCCTGGAGAGAAACGCCCAACAGTACCAGTA[T/A]CTGGTCAAGGTGAGAGACTGACCTCGCTTGATATGATACAGCAGATGTCTATAGAGAAACCAAAACTGGCTTAAAAAAAAAGCTGGGGTTTTGTAGCCATTTCACATGCTTCAGATTCAACTCATTTCCTGCAAAAAATACTTTTATAAAACAAGTATAAAAAAAAAGTGTAAATAAAAAAGTATAAATACTTTTACAAAAAATAGAGTTTTGCTTACCTCAAAATAATCTACCACTGGGGTAAGCAAAATAACTTCTTTAAAAAACATTGACAACTTCTTTATTTATATAGTACATGCATTAAAACATTATAAATATATGTTGAACAAGATAAATAAAACAGATTTGAATTCAAATTTCAGCAAACAAACACCCTTTATTCGTTTATTCCTTTATTAAGATGTTCATGGTAATGTTTACTTTCACCGTTTCATTTAGGGAAACTCCTGAAATAAATATGTTATATCTCTGAACTTTATTAATAAATCTAAATAAAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7408
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 |
---|---|---|---|---|---|
ENSDART00000087926 | Missense | 719 | 1028 | 21 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 27690050)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 28408290 |
GRCz11 | 15 | 28341166 |
KASP Assay ID:
554-4077.1 (used for ordering genotyping assays)
KASP Sequence:
AGCCACCCAACTTCAGTCATCCTGGAAGGGCTACAGTCAAAAAACCAAAT[A/G]CCAAAAAATGCGGCACTCGGCTGTCTGGATCCAAGCCTGGTGGAGAGGAA
Long Flanking Sequence:
TTTTACCAGTAAACAATAGCTGAAAGAAACCATATTTTGAACAAAACTACATCAGTTGCTTATCATCTATACATTTTCTGTGTCTACTGGTCAAAACAGGCCTGAACGCATTGCTAGGATTAATGTTTTAACATTAGTATTATTCATCTAGAACCAAAATTGATGGAGACAACTTTCAATGTAAATAACAAAATTAAACTTTAACTCTAGAACTTCTATGTTAAGCTGCTTTAACACAATCTAGATTGTAAAAGCGCTATAAAAATAAAGATGAATTGAATTGAATGTATTTTTTAAAGGACCAAAATCTTCATCCGCTTCCCCAAGACCTTGTTTGCCACTGAAGACGCACTAGAAGTCAGGAAACACAGTCTTGGTATGAGCTGTTTTAAATACAAATCATGCCCACTGGGTGGTCTGCCTAATGTTAACCTTCACAAACTGTCCCTCAGCCACCCAACTTCAGTCATCCTGGAAGGGCTACAGTCAAAAAACCAAAT[A/G]CCAAAAAATGCGGCACTCGGCTGTCTGGATCCAAGCCTGGTGGAGAGGAATTCTGGCCCGCAGGGCAGCAAAGCGCAGGAGAGAGGCTGCCGACACCATTCGCAGGTCTGTCATACAAGATGGTCATCCTTAAAAGGGACCTATTATGCTCCTTTTTACAAGATGTAAAATAAGTCTCTGATGTCCCTAGAGAGTATATGTCGGCTTGAAATACAACACAAATAATTGTTTTAAACTCTTTAAAACTGGATCGTTTAGGCTTTGATCCTAATTGTGCCATTTTGGTGACCATTTTGGTGTAGCCTTTGTCTCACCATAGCGGCAGATTTAAAACTCTAAAGGTGGACGCTGCTTCTCGCTCAGGGCTGTTTATGCTAATGATGGAGAGATCGTCACTAATGAGCGGGGCTTTCCCCTTCTGATAACATGTAACAAAGGGAGAATGTGAATCAAACTGTTTCTGCAGACTGTTTTAATCAAGTGTGATTAAAAAAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12270
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 |
---|---|---|---|---|---|
ENSDART00000087926 | Nonsense | 904 | 1028 | 26 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 27692501)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 28410741 |
GRCz11 | 15 | 28343617 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTTCCAGTCATTAAGTATGACCGAAAAGGATATAAAGCACGCAACCGA[C/T]AGCTCCTGCTCATGTCTGACAGTGCCGTWATTGTGGAGGAGGGCAAACTC
Long Flanking Sequence:
AGCAGAAAGTGGTTGCGAGTAAAATCTTTAAGGACAAGAAGGACAACTATCCTCAAAGCGTCCCAAAACTTTTTGTGAACACAAGGCTCAGTGAGTTTTCAGTCACTATTATCAAGCTCAATTTAGAGATGCGTTGTATATTCTAAATGTTCTTTTGTGTGTTCAAAAGATGGTGAGGACATCAATCCTAAAGTGCTGCAGGCTCTGGGAAACGAAAAGATGAAGGTCAGTTGAATTCTGGACAGGCTATTTTGGAAATCTTTCTTTAATGTGATTCAAAAATCCATGAATCTGTCATTTTACATAATTAATTGTGAAATATTGCTTATTAGCCTACTTTGTTTCTTCAGAAAACAAAACAAAAATCCCAAAATGTGAAGCATGTGATCATAGACAGTATGTGAGTCTGCTAATGTAATCTAACCTTCATCCGTCCTTCCCTGTAGTATGCTGTTCCAGTCATTAAGTATGACCGAAAAGGATATAAAGCACGCAACCGA[C/T]AGCTCCTGCTCATGTCTGACAGTGCCGTTATTGTGGAGGAGGGCAAACTCAAACAGCGGATCGACTACAACTCACTGAAAGGTGAGAAGGAGGAGGGATAGAGCTTAAATATGAATAGTAGTTTAACCTAAAAACTACAGTTAGGATTTATGTGAACATTTTGCAATGACAGATTTTTTTCCGTTAAACCTTGTGGCATTTGTAGTAATCACTCTTTCAGATTTAAAATTGTTGGAACAAGATGGTGTTTTAATCATCCAATGTTATTTACTTATTTACTGTTAGCAGTAGTCCGTTTACTGGTATTTGTGCCTTCATTCATTGACCAAAAAAAAGCATGTCTTGTAGAAATGTATATTTTGATTGTAGTATGTGTGTTTTAGTAGAACTGCTAGGACTTTTTCAAATATAAGAGCTGGTTAACGGAGGGAAGATTTTTTAAACCCATTTTTAAACAAAGTTTTAATAAATATTTAGCATTTCCTAAATCCATCGTTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44824
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087926 | Essential Splice Site | 1020 | 1028 | 29 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 27698736)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 28416976 |
GRCz11 | 15 | 28349852 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCTCAGAGTTGCTGATAGTCAAGGCTAAGAATGGACACCTTTCTGTG[G/A]TGAGCAAATACATTTGAATCTATGCTTATCTAAAAATAATTCAAATCAAA
Long Flanking Sequence:
GAGAGTTGGTTTTGTAACAAAATTCTGCAAACTAAAACCCCCCATGACACAGACTACACAAACAGGTAACACAATATCCTTCCGCATGCATATGTTATGTGCAATACACAAACTAACCAATTGCCACCAACAAACTCAAAAATCATTAGCCCCATTTGAATGTTAAGACTTTAAAGTTTAGCTCTAGGGTAACATTTTGATGTGACTCAGTTTGTAGAGAATTGGTGGCAAAACGACAACCAAACAATGCAAAAATAAGTACATTTATTTACAAAATCGAAAAGAATTCAAACAGCAAAATAATATGTACATGTTTATATAACAAAAACTCCAAACTGGCTGATTATTATCCTTTAAACTACCTAATAGAAATATGCTTTGCTTTTTCTCTGATGAACAGTATAAAGTTCGATGTGGCACAGGGAAAAGAAGGGATCATAGACTTTACAGCTGGCTCAGAGTTGCTGATAGTCAAGGCTAAGAATGGACACCTTTCTGTG[G/A]TGAGCAAATACATTTGAATCTATGCTTATCTAAAAATAATTCAAATCAAAAACAGTGTGAATAACAGCATGTTTGTATTCGTCAGACCGCCCCTCGCCTCAACTCAAGATGATGGACGAGTCGTGACCAAGCACTTCCAGATACGCTCCTTAGTTCTTCAATCACATGACTACAGGCGGAGCTTTTCTCCACCAATCAGACGCCGGCCAGCCAGCCGCACCAAAGGCCTCTGCTTTCAGTTGCGAAAATCCAGCAAACTTATTTATGTTTTGGGGGATTAATACTGCTATATGAATATATGATTTTATATGTCGAAGCCAAGAAATAACAATATATGTATGTGCATTTTTTCATCTTTATCTAGCTTATTTGGGGGGTGTTGAATGATTTGTTAGAGACGGTGACCTCAGCCATGATCACGAGGTAAATCAGGGTTCACAATTAGCTTTGGTCCTATTTATGATTCTTTTTGCAATCCAAACCCACTCAGAACCAGTACA
Associated Phenotype:
Not determined