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
Note
None
Comparative Information
Expression
All Expression Data
2 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
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 ndufa13 Human Ortholog
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
Associated With ndufa13 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR009346 GRIM-19
Domain Details Per Protein
Protein Length GRIM-19
UniProtKB:Q6PC49 144
Transcripts
Genome Browsers
No data available
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Citations