Gene

slc38a3a

ID
ZDB-GENE-070615-25
Name
solute carrier family 38 member 3a
Symbol
slc38a3a Nomenclature History
Previous Names
  • zgc:165543
Type
protein_coding_gene
Location
Chr: 11 Mapping Details/Browsers
Description
Predicted to have amino acid transmembrane transporter activity. Predicted to be involved in amino acid transmembrane transport. Predicted to localize to integral component of plasma membrane. Orthologous to human SLC38A3 (solute carrier family 38 member 3).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
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 slc38a3a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
developmental and epileptic encephalopathy 102 Alliance Developmental and epileptic encephalopathy 102 619881
Associated With slc38a3a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR013057 Amino acid transporter, transmembrane domain
Domain Details Per Protein
Protein Length Amino acid transporter, transmembrane domain
UniProtKB:A5PLD2 189
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