ZMP
myo1hb
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate myosin IC (MYO1C) [Source:UniProtKB/TrEMBL;Acc:B8JLK6]
Mouse Orthologue:
Myo1h
Mouse Description:
myosin 1H Gene [Source:MGI Symbol;Acc:MGI:1914674]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31456 | Nonsense | Available for shipment | Available now |
sa1578 | Essential Splice Site | Available for shipment | Available now |
sa45209 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33637 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31456
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112968 | Nonsense | 57 | 1021 | 2 | 31 |
ENSDART00000142826 | Nonsense | 57 | 993 | 2 | 30 |
Genomic Location (Zv9):
Chromosome 5 (position 33598506)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 31360738 |
GRCz11 | 5 | 31960891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTTAGACCTACATTGGGACCCTTCTGGTGTCAGTTAATCCATATAAA[G/T]AGTTGGGTATCTACACCAAGAAACAAATGGACATTTACATGGGAGTCAAC
Long Flanking Sequence:
TGAAAAACCTCACATACGAAACTGATGAGGAGTCATATTTACTTATTGTTCATCTTTAACCAATTAAAGTTCACATATGCTGGCAGATCCTTTCATGAGAAAAAGTTAAAATCATATACATCATATTTACTACATATTCATAAACTTCATAACTACTTAGGCAAAAGACTGGCTTTTTACTTCTGGGAAAACTTTATTTTGATGGTCCATTTGAGTATTAGCAGACTGTCTGCTTAATATCTGCTGATACTGCTTCTTCAGCAGACATTTAACTGACTATAAGAAACTTTGCAAGTACATGTCAACTTACACTTACCCCAACCTAACAGTCTACTTATAATCTAATGAGAATTAGTTGGCATGTACATGCACTGTAACTAAATTCAACAAACAGAGCATCAAAATCGAGTGTGACCTAACTTTTTCTTAAATGTGCTTGTTTTTCTCTTTTCTGTTAGACCTACATTGGGACCCTTCTGGTGTCAGTTAATCCATATAAA[G/T]AGTTGGGTATCTACACCAAGAAACAAATGGACATTTACATGGGAGTCAACTTTTTTGAGCTGCCGCCTCATATGTAAGTTTTCATATAATCAAAGGAAAGACATATAACTGTTATAAATAAAAAATGTGTAATAATAGTACCATATGACGAAAATCTAAAGACTTTTTAAATTTCTTCTAAATTTGTTCATATTTTTGACAAATTAAATACGATTATTTTGTACACGTTTATTTCAGAGTACATCATGCTGTGTGTGTGTTTGAGAGAGAGCAGGAAGTAACACCAGCTGTTAAAAATCAGACCAGAGCTCATTAATATTCACGACCTTTCCAAATATGGTCAATATGGAATTTCATTCTAGGGGTAATTTTTGGGCTTTTAGCATATAAATCCATTTTTGGGAAATCTTGTAAGTTGCCTAATGCTGCGTTCACACCAGACGTGGATGAAGCATCAAGCGCAAGTGATTTACATATTAAGTCAATGCAAAGATGCGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1578
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112968 | Essential Splice Site | 561 | 1021 | 16 | 31 |
ENSDART00000142826 | Essential Splice Site | 535 | 993 | 16 | 30 |
Genomic Location (Zv9):
Chromosome 5 (position 33607560)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 31369792 |
GRCz11 | 5 | 31969945 |
KASP Assay ID:
554-1521.1 (used for ordering genotyping assays)
KASP Sequence:
GCATTGCTTCCACACTATTGAGCCTGATGGCAAGAAAAGACCCGAGACGG[T/C]ACAGTAAAATGATATGTGACAAGTGAATGCATTTTTAATGATGATTTTCT
Long Flanking Sequence:
CCTGGAACGAGGAGACTTCAGACTTCTACACTATGCTGGAGAGGTTACTTACTCGGTTGTTGGTAAGTCAACACGCTTTGTGTCAGCTTTTTTAATTTAATAAATTTGTATTTTTGGAGCTTTGGTGTTGCCGCCTTTGATGAATATTTCATTTGCACCTGCGTTTTTTGGCTGAGCACTAAGTTAAGAGGGATTCTTTTGTACAGTTTTTCAAGTCTTTCGTTGCAACCAGTTTTAAGACTAACAAGTCTTTTTCCTTAACTTGACCTGTTTGATTTCCATATGTCAGGATTTCTGGACAAAAATAATGATCTTCTGTACAGAAACATTAAAGAGGTAAGAGATTCCTCCTCTGCATGCATTTACTGTTTGCTTCTCGTCTCTTTGAAATGTTAAAGTTGTTTGTTATTTTGTTAAGGTCATGCGACAGTCTAAGAACAGCATTATCCAGCATTGCTTCCACACTATTGAGCCTGATGGCAAGAAAAGACCCGAGACGG[T/C]ACAGTAAAATGATATGTGACAAGTGAATGCATTTTTAATGATGATTTTCTGGATATAAAAAAAGAATTGTTTAACTGCAGATTTAGTAAAGCTTATTAATAGTGCACCATTTTAATATACTTCTATCAAATAGATATTGTTGACCGCTGTAAGAAAAAAAATCATGCAAAGTTTATTGCAGCATAGTAGTCACTAAGTGCATGGCAGCACCTTGGGCTCAGCAGATTTGCATAGAATCTTTAACATCCTAAGCTCAAACCTTTCTTACAGTTTTAGTTTAGACCTGAAGTGTGCATGATATCAAAATCTACAATGTTTGTTTTACTGGTGCACATTGTTAGTCTTAAGATGAAAAATTAATCTTTGCAAGTTAATCCACCGAAAAACTCCATATGCTTCTGCTTTGGAATGACAGTTCTTGTCTGATGATGTCAGATTGATGACCTGGGTAAAATATGCTTAGCCACAACCCTCCATTGCTAACTGTCAATTTGCTGCAG
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:
sa45209
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112968 | Nonsense | 807 | 1021 | 24 | 31 |
ENSDART00000142826 | Nonsense | 781 | 993 | 24 | 30 |
Genomic Location (Zv9):
Chromosome 5 (position 33614560)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 31376792 |
GRCz11 | 5 | 31976945 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTTTATTGTATTTTATTTTTTCTTTTCTATAAATGAATCTACAGGCCT[C/A]GGTTCTCTTGCGTAACCTGTACACACGCCTCCTTGTTAGGAAGTATGTTC
Long Flanking Sequence:
TAATTTACGTAGCCCATTGCTGACTATTTTGCTTAACTTTATTTTAAATTTTATTCCCGAAAACAAAACATGTTTTTACTTGTCTAGAATGTGCTTCATTTCAGATTTGTTTAGATATCTGTACTCTAAATAATACAAAAACTCTATATAGGAAAATCTGTTTTGCAGTTTGTTAAAAATGTAATAGAATCAAGTTTGAGTTTAAGTGTTTCCCTAAAATCTTACAGATTTATTAAGGGCTTCATGAACAGGAATCAGCCTGTAAGCATGGACAACTCTGAATATCTGGCCTTTGTCAGACAGAGCTACCTCACTCGACTCAAAGAGAACCTGCCAAAATCAGTTTTGGACAAAACCACGTGGCTGACTCCTCCACCCATAATGCAGGAGGTAGATCCTTCTTCATTGAAGACAAGTCTTTTTTGAAATTTCATAAGATAAGAATCATAAGATTTTATTGTATTTTATTTTTTCTTTTCTATAAATGAATCTACAGGCCT[C/A]GGTTCTCTTGCGTAACCTGTACACACGCCTCCTTGTTAGGAAGTATGTTCGAGGGATCAGCGCACAGAGAAAGATGCAGGTAAAATTGTGTTTTTCACCTCTCATTTATCTGAACATTTATTATCCTACTACATTCTCTGATTGTATATGTTTAATACTCCTATTTTATTTACAGCTGCAAACCAAAGCACTGACCAGTGAAATTTTCAGAGGCAGAAAGGAGAGCTACCCTCAGAGCGTATGCCAACCCTTCGCTGACACTAGGATAAGTAAGAATTTGTCATTTTTTTTCTCAACTATTGCAAGCTACTATTAACTTTGCAGTGTGTAAATCCAAAGGTTACAAATAAACAACATTGTTTTTTGGTTGTCTTCAGGTGAACAGGACATAAACATTAAAGTCTTACAACTGATTTGTCCTGAAGGCATTAAGGTTAGTAAAACTATGAGCTATTCTAGCACTTTTAACAACAAAGTCCTTATATATACACTGTTTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33637
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 |
---|---|---|---|---|---|
ENSDART00000112968 | Essential Splice Site | 928 | 1021 | 27 | 31 |
ENSDART00000142826 | Essential Splice Site | 902 | 993 | 27 | 30 |
Genomic Location (Zv9):
Chromosome 5 (position 33616847)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 31379079 |
GRCz11 | 5 | 31979232 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGGAGGAGGCCAAAATCAAACAGAGGGTGAATTACAGCTCTCTAAAAG[G/A]TCAAATTTCAGTGTTGTTCATTAATTAAACATCTCAAATTGTGTGAAATG
Long Flanking Sequence:
ATATTATGCACAGTTACCATGGCAAACACAGAACAAATTAGTTATTAGAAATTAATTGTCAAAACTATTATATATGTTGAAAAACTCTTCTCTCCATTAAACAACACTTGAGAAATGTTTTTAAAATAATAAAAATTTCACAGGAGGACTAATAAAATATGAACATGAATTCATTTGTTGGGTGTAAACATATTTCTGTTTTATTCATAAATCATATTTCTGTTCCTGCTGCAGGAATACTTAGTTAAATGTCTGTAGGTGTTTAACTCAAAGTGTAGTAGACACTGGAGTTTTATTTGTTAGTTGGACAGATGTTTATGTCACTGGTATGAAAAAAGTGATTGTGTTATCTCCCTCTGTACAGTACAGTGTTCCAGTGATTAAATATGACAGGAATGGCTTTCGTCCACGTTTCAGACAGCTTATCTTCACTCAGGCCGCTGCGTATCTGGTGGAGGAGGCCAAAATCAAACAGAGGGTGAATTACAGCTCTCTAAAAG[G/A]TCAAATTTCAGTGTTGTTCATTAATTAAACATCTCAAATTGTGTGAAATGTCCAATTAATTCATAATCCATGGGTATTTTTATTTATAAATGTATGATATTTTGATATTATTAATATTAATATCCAGCAATAATTTTTCTTCTGTCTTGCCTACAACATGGCTACATTTTGGCTGCCAGTTAAAATCTATCTGACTTTGAAAAACAGTCCAAAAATAGATTAGTTTTCTATTAGAGTTTCAATGACAGGCCAAATTCAGCCTTGTTTTAGCCAAGATGTCTATTAAACTAAATGGTTTAGTGGAATATAAAACTAGAATTTGATATTTCATTTAGAGATGTGTAAATATACCTCTTGATGTAGTTTTGTTTTGTTCAGACTATGTTGTTTATTTAGTCCTATTTTAATCCTTTTAACAGTCCTGTAACATGTCACTGCTAAATTAACCAGTACAGTAGACAAAGCATAATGTTAAAAATAAATCTATTTGTTTACAGTAA
Associated Phenotype:
Not determined