Gene
ndufa13
- ID
- ZDB-GENE-040426-1672
- Name
- NADH:ubiquinone oxidoreductase subunit A13
- Symbol
- ndufa13 Nomenclature History
- Previous Names
-
- zgc:73107 (1)
- Type
- protein_coding_gene
- Location
- Unmapped
- Description
- Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in mitochondrial complex I deficiency and thyroid gland Hurthle cell carcinoma. Is expressed in intestine. Orthologous to human NDUFA13 (NADH:ubiquinone oxidoreductase subunit A13).
- Genome Resources
-
- Alliance (1)
- Gene:393687 (1)
- Note
- None
- Comparative Information
-
- All Expression Data
- 2 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:73107 (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 28 | Alliance | Mitochondrial complex I deficiency, nuclear type 28 | 618249 |
| oncocytic carcinoma of the thyroid | Alliance | {Thyroid carcinoma, Hurthle cell} | 607464 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR009346 | GRIM-19 |
Domain Details Per Protein
| Protein | Length | GRIM-19 |
|---|---|---|
|
UniProtKB:Q6PC49
|
144 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance