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 be involved in mitochondrial respiratory chain complex I assembly. Predicted to localize to mitochondrion. Human ortholog(s) of this gene implicated in nuclear type mitochondrial complex I deficiency 29 and optic atrophy 7. Orthologous to several human genes including TMEM126A (transmembrane protein 126A).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Thisse et al., 2004
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 tmem126a Human Ortholog
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
Associated With tmem126a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR009801 Transmembrane protein 126
Domain Details Per Protein
Protein Length Transmembrane protein 126
UniProtKB:Q6PBL7 201
UniProtKB:A0A2R8QM83 206
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
Gene Tree
Ensembl
Citations