Busch Lab

ZMP

NP_001155104.1

Ensembl ID:
ENSDARG00000062003
Description:
myosin-Vb [Source:RefSeq peptide;Acc:NP_001155104]
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
sa43638 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa43638
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000089030 Nonsense 1590 1839 37 41
Genomic Location (Zv9):
Chromosome 21 (position 21406558)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 22417980
GRCz11 21 22454616
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCTGGCGGAGTACCGACAGGTTCTGAGTGACCTCTCCATCCAAATCTA[T/A]CAGCAGCTTGTGAAAGTTGCCGAGGCCAACATGCAGCCCATGATCGGTAG
Long Flanking Sequence:
ATCCTTTCCTTTTCTGACTGTAAATGTCTGGTCGCTGGAATCATGTGGACAAACACAGTAGGGTACCAAGCCCTATTTGTTAAAAGTTGATATACATGAATCTGAATTATAGAGTGTCCTATGTGTATCACCCATGGCTTTCCGATCTTTGTTTATTTTTTTAATAAACAGTGTGAGATGTCATGTGATGTTGTTCATCTGAGGTGTTATCTTTCAAATTTTAAGACCTACCAAGCAGTTTTTTTTAATGTCTTGAAACTAAAAAACCTGAAATTCAATAGGGTGTCTTTTTACACGACTGTAGTTACTTAAAATAAGCCAATAGTCCACAGGGGAGCATCAAAAATAAAGTGTAACCAGTGCTCGGTATGATTTGCCTGTCTAATTCTGTCCTAGGCGTTCATGACCCAGAACTCTGCCAAGCAGAACGAGCACTGCCTGAAGAACTTTGACCTGGCGGAGTACCGACAGGTTCTGAGTGACCTCTCCATCCAAATCTA[T/A]CAGCAGCTTGTGAAAGTTGCCGAGGCCAACATGCAGCCCATGATCGGTAGGTGCAGAGAGACACCAAACCAAAGAAGATTGATCATTAGCACAGTACATTTTTTCATAATGAGTGTGTTTTGTAGTGTCTGCCATGCTTGAGAGCGAGAGCATCCCCAGCCTGGCCGGAGTGAAGCCCATGGGTTACAGGAACCGCTCCTCTAGTGTGGACTGTGAGAGTGGAGGTCCCGCAGGATACACGCTTCAGGCACTGATCAAACAGCTGGCTCAGTTTTACTCTACCATGGCGGACCACGGCCTGGACCCTGAGATCAGCCAGCAGGTGCTTCGCCAGCTCTTCTACTCCATCAACGCAGTGACCCTCAACAACCTGCTGCTGCGCAAGGACGTCTGCTCCTGGAGCACCGGCATGCAGCTCAGGTACACATTTTTAATGCTTTTAGGCTAATTAATATTTTTCTCAGCAGTCATCATAGTTAGGTAAACTTAAAGAGCAGTGA
Associated Phenotype:
Not determined