Gene
tmem126a
- ID
- ZDB-GENE-040426-1770
- Name
- transmembrane protein 126A
- Symbol
- tmem126a Nomenclature History
- Previous Names
-
- zgc:73348
- Type
- protein_coding_gene
- Location
- Chr: 10 Mapping Details/Browsers
- Description
- Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in mitochondrial complex I deficiency and optic atrophy 7. Orthologous to several human genes including TMEM126A (transmembrane protein 126A).
- Genome Resources
- Note
- None
- Comparative Information
- All Expression Data
- 1 figure from Thisse et al., 2004
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- IMAGE:7137105 (1 image)
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 |
---|---|---|---|
nuclear type mitochondrial complex I deficiency 29 | Alliance | Mitochondrial complex I deficiency, nuclear type 29 | 618250 |
optic atrophy 7 | Alliance | Optic atrophy 7 | 612989 |
Domain, Family, and Site Summary
Type | InterPro ID | Name |
---|---|---|
Family | IPR009801 | Transmembrane protein 126 |
Domain Details Per Protein
Protein | Length | Transmembrane protein 126 |
---|---|---|
UniProtKB:A0A2R8QM83
|
206 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available