Gene

myo15ab

ID
ZDB-GENE-090312-149
Name
myosin XVAb
Symbol
myo15ab Nomenclature History
Previous Names
  • si:ch211-201p7.8 (1)
Type
protein_coding_gene
Location
Chr: 1 Mapping Details/Browsers
Description
Predicted to enable ATP binding activity; actin binding activity; and cytoskeletal motor activity. Predicted to be involved in system development. Predicted to be located in cytoskeleton. Predicted to be part of myosin complex. Is expressed in neuromast and otic sensory epithelium. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 3 and sensorineural hearing loss. Orthologous to human MYO15A (myosin XVA).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Erickson et al., 2015
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With myo15ab Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal recessive nonsyndromic deafness 3 Alliance Deafness, autosomal recessive 3 600316
Associated With myo15ab Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
Protein Additional Resources Length
UniProtKB:A0A8M9Q2K6 InterPro 4355
Transcripts
Genome Browsers
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA myo15ab-201 (1) Ensembl 7,128 nt
mRNA myo15ab-202 (1) Ensembl 438 nt
mRNA myo15ab-203 (1) Ensembl 498 nt
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations