Gene

slc25a26

ID
ZDB-GENE-050913-126
Name
solute carrier family 25 member 26
Symbol
slc25a26 Nomenclature History
Previous Names
  • SAMC (1)
  • zgc:110080
Type
protein_coding_gene
Location
Chr: 11 Mapping Details/Browsers
Description
Predicted to have S-adenosyl-L-methionine transmembrane transporter activity. Predicted to localize to mitochondrial inner membrane. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 28. Orthologous to human SLC25A26 (solute carrier family 25 member 26).
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 slc25a26 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
combined oxidative phosphorylation deficiency 28 Alliance Combined oxidative phosphorylation deficiency 28 616794
Associated With slc25a26 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Homologous_superfamily IPR023395 Mitochondrial carrier domain superfamily
Repeat IPR018108 Mitochondrial substrate/solute carrier
Domain Details Per Protein
Protein Length Mitochondrial carrier domain superfamily Mitochondrial substrate/solute carrier
UniProtKB:A0A2R8S0H9 238
UniProtKB:Q4V9P0 267
UniProtKB:E9QJ99 170
UniProtKB:B2GQ56 267
Transcripts
Genome Browsers
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