Gene

slc25a22b

ID
ZDB-GENE-110408-66
Name
solute carrier family 25 member 22b
Symbol
slc25a22b Nomenclature History
Previous Names
  • si:ch73-219d10.1
Type
protein_coding_gene
Location
Chr: 7 Mapping Details/Browsers
Description
Predicted to have L-aspartate transmembrane transporter activity and L-glutamate transmembrane transporter activity. Predicted to be involved in L-glutamate transmembrane transport; aspartate transmembrane transport; and malate-aspartate shuttle. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in early infantile epileptic encephalopathy 3. Orthologous to human SLC25A22 (solute carrier family 25 member 22).
Genome Resources
Note
None
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
No data available
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 slc25a22b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
developmental and epileptic encephalopathy 3 Alliance Developmental and epileptic encephalopathy 3 609304
Associated With slc25a22b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR002067 Mitochondrial carrier protein
Homologous_superfamily IPR023395 Mitochondrial carrier domain superfamily
Repeat IPR018108 Mitochondrial substrate/solute carrier
Domain Details Per Protein
Protein Length Mitochondrial carrier domain superfamily Mitochondrial carrier protein Mitochondrial substrate/solute carrier
UniProtKB:A0A2R8QSJ0 352
UniProtKB:F8W3S7 318
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Gene Tree
Ensembl
Citations