ZMP
myo5aa
Ensembl ID:
ZFIN ID:
Description:
myosin-Va [Source:RefSeq peptide;Acc:NP_001074428]
Human Orthologue:
MYO5A
Human Description:
myosin VA (heavy chain 12, myoxin) [Source:HGNC Symbol;Acc:7602]
Mouse Orthologue:
Myo5a
Mouse Description:
myosin VA Gene [Source:MGI Symbol;Acc:MGI:105976]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23354 | Essential Splice Site | Available for shipment | Available now |
sa23355 | Essential Splice Site | Available for shipment | Available now |
sa36702 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23354
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088037 | None | None | 1891 | None | 42 |
ENSDART00000088038 | None | None | 1843 | None | 40 |
ENSDART00000121644 | Essential Splice Site | 584 | 1890 | 16 | 44 |
ENSDART00000133618 | None | None | 1844 | None | 39 |
Genomic Location (Zv9):
Chromosome 18 (position 37423242)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 39004945 |
GRCz11 | 18 | 38985953 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGTCTATGTGTTGTATGTGAACATGACAACCTGTACCCCTGCAGAAGG[T/A]AAAACTCAGCCTATAAATGCACTCTTTAGCGCTATAATCTATCTAATATC
Long Flanking Sequence:
TAAAATAAGTGTAATCTAGAGGCCTATGCCTTTCATATAAGCCACTTTTCATATCAAATGATCAACTAGAAGTCAAGTTATTATTTGTTGTTTCTAAAACTTGGATAGGCGACAAGACTTTTGTCAGGTAGTGTATATTTTAAATAGCCAGAGTGTGATTAAATTAACAGCAACCTTGTTTTTGGTTAAACCTTGCTTTTAAGAGGGATTTCACATTGCATGCACATTGTATTCTCAGGTTTTGGGATTTAGAAAATATAGATAATCTATTATTATTATTATTATTATTATTATTATTTTTTTTTTTTAAGCATACTGGATTTGTCAAGTCAACATTATGTTTCCAAGCTGGTGTCTGAGCTGCTTCGCTGTTCAAGTACACTACATCTGTCTTATGTATCTGTATTTTCTGCTTTTGTTAATTCTGTTTCTGTTTTCTCATCATGTCATGTTGTCTATGTGTTGTATGTGAACATGACAACCTGTACCCCTGCAGAAGG[T/A]AAAACTCAGCCTATAAATGCACTCTTTAGCGCTATAATCTATCTAATATCACAGTTTTGCAGTAGCTACAAATACTAAGATGGAATGCATGTTAACAAGTGTGTGAGTGTGCGCGTGTGTGTCAGCATGTTGAGTCTGTTGCTTTCTGCAGTGCAGGACAGAATCTTATTGAACACTGCACTGATTCTGTAGGAAAATAAACTGGCTTCAGCTCTAGAGCCCACACTCCATACAAACAAACTCGGCTGCTTGGATAGAACGACGCATCTGTTTAGATTAAACAGACATTAATGCTCTTAAAGGGACTGTTCACCCAGAAATGAAGATTCTGACCATTTTTATTCATTCTCAGTTTATAGTAAAAAGTGAAAAAGCAAACAGTTAAGGCCATGTCCACACTTAAAGTGCTATATTTATGAAGGGAGTTTTCCATGTTTTTCAATGCAAACAGAACAGAGGTGGAATACTCTCCAGCGGTCGAAAAATGTGGAACAAACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23355
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088037 | Essential Splice Site | 1282 | 1891 | 28 | 42 |
ENSDART00000088038 | Essential Splice Site | 1302 | 1843 | 29 | 40 |
ENSDART00000121644 | Essential Splice Site | 1281 | 1890 | 30 | 44 |
ENSDART00000133618 | Essential Splice Site | 1303 | 1844 | 28 | 39 |
Genomic Location (Zv9):
Chromosome 18 (position 37454669)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 39036372 |
GRCz11 | 18 | 39017380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCCTGCGCTCACAGCTCGTCAGTCAGAAAGAAGCCATGCAGCACAAG[G/A]TCAGATGCCAAAACTCACATCAGGACTCATATCTGCTCAAATCTGTCACT
Long Flanking Sequence:
CATATTGTTGAGTTACTGAAAAACTCCAAAGTATTTTTCCAAAATTTTTGTCAAAATAAGATTTGTCACCAAAAGTGACTCCACTTGCTTCTACAAACAAAGAACGTTGTGGCCAAATTAAGATTTAAAATCAACTCCGCATGGATGAAAACAACCCCAACTGCACACAAGGGATAACTTGAAGGCATCATTAACAAATCTATATTTAGCATGATCCTGTAACTCTTATATTTTTTTGCATGTTGATAATTCTGAACATCTTAAATCTTCAGCGTCAGGAGCTGGAGTCTGAGAACAAGAAGCTGAAGCATGATCTGAATCAGATGCGTCAGTCTCTCAGAGGCAGCGTTGAGGCCGGTTCTGGTGCTCCTGGTTCTCCTGCGTACACCGTTCTTCTGGATCAGCTCAATGCCTCCAACGAGGAACTGGAAGTGCGCAAAGAGGAGGTGCTCATCCTGCGCTCACAGCTCGTCAGTCAGAAAGAAGCCATGCAGCACAAG[G/A]TCAGATGCCAAAACTCACATCAGGACTCATATCTGCTCAAATCTGTCACTAACATTCTACTCTTCTTGAGTGTTGTTGACATTTCTAACTTTTGACTCATTTCTGCTTTTGTCTCGTGTTGCATTCATAACAGGATGAGAAGGTATGTTGGTCAGACAGAATAACAGTCATTTTACATCAGTTTGTGTCTCTAAAATGTTATTGTTTAGTGTTAAGGCGGCCACTTTGAAATATTAGCTTTCAAAAATAGAAATGATTTGTTTGTGTTTAGTTTTGAGTAAGTGAAAGAAATGTTTTTATAGGGTCTAAAAGTCTCCTATAAAGTAAAGCTTTATAGTAAAAAAACAACAACAACATAAATGTGTTTATTTTCTTTTACTATTATAATGATAAAATAAAATAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATTCATTATATTATAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36702
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088037 | Nonsense | 1607 | 1891 | 37 | 42 |
ENSDART00000088038 | Nonsense | 1559 | 1843 | 35 | 40 |
ENSDART00000121644 | Nonsense | 1606 | 1890 | 39 | 44 |
ENSDART00000133618 | Nonsense | 1560 | 1844 | 34 | 39 |
Genomic Location (Zv9):
Chromosome 18 (position 37472771)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 39054474 |
GRCz11 | 18 | 39035482 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTTCTGGTTGGCCAACACATGTCGTTTTCTGCACTGCCTGAAACAGTA[C/A]AGTGGTGATGAGGTGAGAAATCACACACCATCACAAGAATATGTGAAGTT
Long Flanking Sequence:
TCAGCAAATACTCACTCACCCATTTTAAAACCATGTATCCATCAATTCTTATCCCCATTCTAAAATGCCTTAATAAAAGTAAAAAAAGAGGACTATCGCTGACCGCTCCATCTGTAATTTTGCCAGAGCTGAAGCCTCGTGGTGTTGCAGTGAATCTGATACCAGGTCTGCCCGCATACATCCTCTTCATGTGTCTGCGCCATGCTGACTACATCAACGATGACCAGAAAGTGCGATCTCTACTCACCTCCGTCATCAACAGCATCAAGAAGATCCTCAAGGTCTCGAATCACTCACGCAATTCATGTTTATAATGTTGCAACTTACAAAATTTACAAACTGTAAATTTGTATTATAAAAGCATAATCACTGTTAAGAGTAAATAATTAAGAATTGTTGTTTCCCTTTCCCATAACTCCACAGAAACGAGGTGATGACTTTGAGACTGTTTCCTTCTGGTTGGCCAACACATGTCGTTTTCTGCACTGCCTGAAACAGTA[C/A]AGTGGTGATGAGGTGAGAAATCACACACCATCACAAGAATATGTGAAGTTTATTCATAAACTAATTTCTAGTAGATCACATGTTTATGATTGACCTCAGCTGGTCCTGTGTTAGCTAACCACATGATTTACCAATCAGATGAATCCTAACACACTATAAATGACCAGAGTTTCCTACCTTAGTTATCTTCCACCCTATTCCTCCTCCCTTTCCCTTGATAGGGAGGCATGGTGGCTCAGTGGTTAGCACTGTTGTCTTACAGCAAGAACGTCACTGGTTCAAGTCCTTACTAGGCCAGTCTGTGTTTCTGTGAGGAGTTTACATGTGCTCACATGGGTTTTCCCTGGGTTCTGCCGTTTCCTCCAACACTCCAAAGACGTGACATAAGTGAATTGACTAAACCAATTTGACACCATAGATGAGCTCCTACTTATGCCTTTCAGTCAGCAGTTTATATCTCCCTATAATCTCTCTTAGGTTCTACATAAACCAGGGGAGTT
Associated Phenotype:
Not determined