Gene
elovl4a
- ID
- ZDB-GENE-040426-1767
- Name
- ELOVL fatty acid elongase 4a
- Symbol
- elovl4a Nomenclature History
- Previous Names
-
- zgc:73341
- Type
- protein_coding_gene
- Location
- Chr: 16 Mapping Details/Browsers
- Description
- Predicted to have fatty acid elongase activity. Involved in very long-chain fatty acid biosynthetic process. Predicted to localize to integral component of endoplasmic reticulum membrane. Human ortholog(s) of this gene implicated in corneal dystrophy and spinocerebellar ataxia type 34. Is expressed in several structures, including liver; nervous system; neural rod; pleuroperitoneal region; and trigeminal placode. Orthologous to human ELOVL4 (ELOVL fatty acid elongase 4).
- Genome Resources
- Note
- None
- Comparative Information
- All Expression Data
- 10 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:73341 (6 images)
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 |
---|---|---|---|
spinocerebellar ataxia type 34 | Alliance | Spinocerebellar ataxia 34 | 133190 |
Stargardt disease | Alliance | Stargardt disease 3 | 600110 |
Ichthyosis, spastic quadriplegia, and impaired intellectual development | 614457 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | ELO family | ELO family, conserved site | Elongation of very long chain fatty acids protein 4 |
---|---|---|---|---|
UniProtKB:Q6PBM2
|
309 |
Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
---|---|---|---|---|---|
mRNA |
elovl4a-201
(1)
|
Ensembl | 2,172 nt |
Interactions and Pathways
No data available
Plasmids
No data available