ZMP
myo5b
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate myosin V family (Myo5) [Source:UniProtKB/TrEMBL;Acc:Q1LWT8]
Human Orthologue:
MYO5B
Human Description:
myosin VB [Source:HGNC Symbol;Acc:7603]
Mouse Orthologue:
Myo5b
Mouse Description:
myosin VB Gene [Source:MGI Symbol;Acc:MGI:106598]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37296 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa3127 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa37296
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000135062 | None | None | 502 | None | 13 |
| ENSDART00000141076 | None | None | 249 | None | 5 |
| ENSDART00000142707 | Nonsense | 1065 | 1525 | 24 | 34 |
| ENSDART00000144461 | None | None | 158 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 21527066)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 22439588 |
| GRCz11 | 21 | 22476224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAGGAGAGCCGCCTGCAGCATGAACTGGATGACGAGAGACAACGATA[T/A]CAGAACCTGGTGAAAGAATATTCCCGACTGGAGCAGAGATACGAAAACCT
Long Flanking Sequence:
AATTCTTGCATACGATGATTTTATTTGTTGAGATTACAAAATGAAGGACATATTGTAACCTACACATAGACGCTCAAAGGTCTTCATTCAGAGTAGTAATAAAAACTTTTATTGATCAATAAAATATCAATCAAGAAAAAGATCAATAATTGATGTGCTATCATCAATGTTATATTGCATAATATTTGGGCTAATAAAAACCTGTAGTTTGCAGGTAAAAACACTCAGTCAAAGATGTCACCGGTTGAATTGATTATAAAGAGTTTTCGGTTTTCTCATACCATATGAAAACCCTCTCATTAGACCTAGATTGTGAGAAAGATGTTGTTCATAATGAAAAAAAAATTCAGCTTGTGAAAGATGATACGAGGGAATGGGATGAGCGTGGCATCTGGTTGATGGTGTTATTTGTGTGTGTTGTGTCTCTCAGATCAGGGAGGTGATGTGTCTCAGAAGGAGAGCCGCCTGCAGCATGAACTGGATGACGAGAGACAACGATA[T/A]CAGAACCTGGTGAAAGAATATTCCCGACTGGAGCAGAGATACGAAAACCTGCAGGAGGACATGTCTTCAATGAAGGTAACAATTTTACAGCGAGACTGATCTTCTGAGGCCTTTTAAACAAATCTGGTTTGGGTTTTTACTCAGGTAAGTTTGCATTTATTTTGAGCAAACAACACAAATGTGAGTTTTGGGGCTGAAAAGGATGGTTTGGTTTTGATCAGGTTTCACTACTTGGCTAAACTGCTTCTGAGAAGCTTTTGTTCTGGGTTAGAGATCACAAACCCAAATTGGACCAATCAGCAGTGAGTAAAGTGACGTGTATATCTGATGCAATAAAGCCACTCCCAGTGACATTTTGTCCAAATTAATGCTTTTTACACTGAAAGGATTTTTGAGTTAAAATTGTGTTGTGATGATAATAGTAATTTATATTGTATGAATTACAATTATTTATATTATATTTGAATATTATATATTTAAATTAGGGCAGTACAATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3127
Status:
F2 line generated
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000135062 | None | None | 502 | None | 13 |
| ENSDART00000141076 | Nonsense | 92 | 249 | 2 | 5 |
| ENSDART00000142707 | Nonsense | 1290 | 1525 | 29 | 34 |
| ENSDART00000144461 | None | None | 158 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 21517222)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 22429695 |
| GRCz11 | 21 | 22466331 |
KASP Assay ID:
554-3228.1 (used for ordering genotyping assays)
KASP Sequence:
TTATTTCATCTGCACAGAATTCCAACGATGTGTCTGAGTGGACCGACAAC[A/T]AGAGCCCTGTGGACRCRGAGGACCGCGTGGATGCGCCTGCATCAAAGAAG
Long Flanking Sequence:
TTTTAAATTCTAGGGTGAACTATCCCTTTAATGCTGCTTTATTGCCAATATTTTCGTTTTTTACTCATAGTTCATCAGCATCACATTAAGCTTCAGTGAAAATATCTTGAATTTTCTTCTGTGAAAGCAGTCAAGCGTGATGATATTGCATGGGATAAAGTGAGCAAAGGAAGGTTTAGTGTATTAAGGATGGAGCTTTGCAAAACCTGCACTGCTAGTGACTTTATATCCACCTGCCTGTGTGAATCTGCTGAGGTTGGCAGATCAGTGACAGTATTGATTATACCCAGATGGAAAGCCCTTTTCTTGTTTTCCCTCAGTTGTATGTCTCTCCCTCAGATATATTTTCCTCTCCAAAAAAATTGTCTCGTTAAAATTGAGAACAATACAGTATACTTTTTCTTTCTGCTTCAGTAAACAAAAATTAATCAATTACCCCCATTGATATCTTTATTTCATCTGCACAGAATTCCAACGATGTGTCTGAGTGGACCGACAAC[A/T]AGAGCCCTGTGGACACGGAGGACCGCGTGGATGCGCCTGCATCAAAGAAGTAAGGCAGTGCAGTCTGCATAATGAAGGGCTTGACACCGGTTCTCCTCCATGCACTTATTTCTGTTTTTTTAATGAAGTTGGAGTATTGAACGCTGGCTATCTGAGTCCAGGGCAGGTCTCTGATTCAGCACTTCATGCTGTGTTTACTTTCATTTTCAGCAGTGAACCTCTGTTTTCTGAACCACATTTTGGGTCATGAATTAGCATAGAGTTAAGCTGCAAACTTAAAGAGGCACTGACAGGTTTGCATGTAAAGGTTGTTCTGTCAAATTTATAGACTTACCAATTATCACTTTATTTATTATTTTTTGTCACTCAGCTTGCATTTTTTTTTGTTCTGTTTGACATTGATTTTATAATATATTAATGTCTGATGATCTAAATCCAATTCAGGTTAGCTTTCAAGAAAACCAACCATATAATTAGTGGCAATAGTGGTTATTTCTTAG
Associated Phenotype:
Not determined