- Gene Overview
- Interaction Network
- Sequence Verification
SLC3A1, solute carrier family 3 member 1
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This gene encodes a type II membrane glycoprotein which is one of the components of the renal amino acid transporter which transports neutral and basic amino acids in the renal tubule and intestinal tract. Mutations and deletions in this gene are associated with cystinuria. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
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Gene Synonyms (neutral and basic amino acid transport protein rBAT, B(0,+)-type amino acid transport protein, SLC3A1 variant B, SLC3A1 variant C, SLC3A1 variant D, SLC3A1 variant E, SLC3A1 variant F, SLC3A1 variant G, amino acid transporter 1, solute carrier family 3 (amino acid transporter heavy chain), member 1, solute carrier family 3 (cystine, dibasic and neutral amino acid transporters), member 1, solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1, ATR1, CSNU1, D2H, NBAT, RBAT,)
- NCBI Gene ID:
6519
- Species:
Homo sapiens (Human)
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UNIPROT ID#>>A0A0S2Z4E1
UNIPROT ID#>>Q07837
UNIPROT ID#>>B8ZZK1
- View the NCBI Database
for this Gene »
Gene products are often involved in multiple pathways and networks within a living
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solute carrier family 3 member 1 interacts with:
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