Gene Name | solute carrier family 3 (amino acid transporter heavy chain), member 1 | |
Image | No pdb structure | |
Gene Ontology Annotations | Cellular Component | |
Molecular Function | ||
Biological Process | ||
Pathways | ||
Drugs | ||
Diseases | ||
GWAS | ||
Protein-protein Interactions | 1 interactors: SLC7A8 | |
Entrez ID | 6519 | |
HPRD ID | 00090 | |
Ensembl ID | ||
Uniprot IDs | Q07837 | |
PDB IDs | ||
Enriched GO Terms of Interacting Partners? | ||
Tagcloud ? | 2p16
aminoaciduria
amplified
another
autosomal
base
belgian
coding
comprising
cystinuria
deletions
described
detect
dscr1
entire
exon
exons
fluorescent
located
making
missing
multiplex
named
rbat
recessive
scanning
semi
ten
transporter
|