Gene

slc25a20

ID
ZDB-GENE-040426-1869
Name
solute carrier family 25 member 20
Symbol
slc25a20 Nomenclature History
Previous Names
  • zgc:77760 (1)
Type
protein_coding_gene
Location
Chr: 22 Mapping Details/Browsers
Description
Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in carnitine-acylcarnitine translocase deficiency. Is expressed in visceral fat. Orthologous to human SLC25A20 (solute carrier family 25 member 20).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
3 figures from 3 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 slc25a20 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
carnitine-acylcarnitine translocase deficiency Alliance Carnitine-acylcarnitine translocase deficiency 212138
Associated With slc25a20 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR050567 Mitochondrial Carrier
Homologous_superfamily IPR023395 Mitochondrial carrier domain superfamily
Repeat IPR018108 Mitochondrial substrate/solute carrier
Domain Details Per Protein
Protein Length Mitochondrial Carrier Mitochondrial carrier domain superfamily Mitochondrial substrate/solute carrier
UniProtKB:Q6P5K6 300
Transcripts
Genome Browsers
Type Name Annotation Method Has Havana Data Length (nt) Analysis
aberrant processed transcript slc25a20-002 (1) Ensembl 757 nt
mRNA slc25a20-201 (1) Ensembl 1,424 nt
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