Gene
myo15aa
- ID
- ZDB-GENE-080425-2
- Name
- myosin XVAa
- Symbol
- myo15aa Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 3 Mapping Details/Browsers
- Description
- Predicted to enable ATP binding activity and cytoskeletal motor activity. Predicted to be located in cytoskeleton. Predicted to be part of myosin complex. Is expressed in midbrain hindbrain boundary neural plate; oocyte; presumptive rhombomere 3; and presumptive rhombomere 5. 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
-
- All Expression Data
- 2 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| autosomal recessive nonsyndromic deafness 3 | Alliance | Deafness, autosomal recessive 3 | 600316 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
myo15aa-201
(1)
|
Ensembl | 12,857 nt | ||
| mRNA |
myo15aa-202
(1)
|
Ensembl | 597 nt |
Interactions and Pathways
No data available
Plasmids
No data available