Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene miRNA Gene ontology Other IDs Protein
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.	157724
Gene name Gene Name - the full gene name approved by the HGNC.	Solute carrier family 7 member 13
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.	SLC7A13
Synonyms (NCBI Gene) Gene synonyms aliases	AGT-1, AGT1, XAT2
Chromosome Chromosome number	8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.	8q21.3

Show/Hide all(13)

miRTarBase ID	miRNA	Experiments	Reference
MIRT018744	hsa-miR-335-5p	Microarray	18185580
MIRT1367122	hsa-miR-3606	CLIP-seq
MIRT1367123	hsa-miR-3908	CLIP-seq
MIRT1367124	hsa-miR-3942-5p	CLIP-seq
MIRT1367125	hsa-miR-4325	CLIP-seq
MIRT1367126	hsa-miR-4522	CLIP-seq
MIRT1367127	hsa-miR-4703-5p	CLIP-seq
MIRT1367128	hsa-miR-4714-5p	CLIP-seq
MIRT1367129	hsa-miR-4766-3p	CLIP-seq
MIRT1367130	hsa-miR-4786-3p	CLIP-seq
MIRT1367131	hsa-miR-507	CLIP-seq
MIRT1367132	hsa-miR-557	CLIP-seq
MIRT1367133	hsa-miR-921	CLIP-seq

Show/Hide all(5)

GO ID	Ontology	Definition	Evidence	Reference
GO:0003333	Process	Amino acid transmembrane transport	IBA	21873635
GO:0015179	Function	L-amino acid transmembrane transporter activity	IBA	21873635
GO:0015807	Process	L-amino acid transport	IEA
GO:0016021	Component	Integral component of membrane	IEA
GO:1902475	Process	L-alpha-amino acid transmembrane transport	IEA

MIM	HGNC	e!Ensembl
617256	23092	ENSG00000164893

Protein

UniProt ID

Q8TCU3

Protein name

Solute carrier family 7 member 13 (Sodium-independent aspartate/glutamate transporter 1) (X-amino acid transporter 2)

Protein function

Associates with SLC3A1/rBAT to form a functional heterodimeric complex that transports anionic and neutral amino acids across the apical plasma membrane of renal epithelium. Preferentially mediates exchange transport, but can also operate via fa

Family and domains

Pfam

Accession	ID	Position in sequence	Description	Type
PF13520	AA_permease_2	15 → 439	Amino acid permease	Family

Tissue specificity

TISSUE SPECIFICITY: Expressed in the kidney. {ECO:0000269|PubMed:11943479}.

Sequence

MDRGEKIQLKRVFGYWWGTSFLLINIIGAGIFVSPKGVLAYSCMNVGVSLCVWAGCAILA
MTSTLCSAEISISFPCSGAQYYFLKRYFGSTVAFLNLWTSLFLGSGVVAGQALLLAEYSI
QPFFPSCSVPKLPKKCLALAMLWIVGILTSRGVKEVTWLQIASSVLKVSILSFISLTGVV
FLIRGKKENVERFQNAFDAELPDISHLIQAIFQGYFAYSGGACFTLIAGELKKPRTTIPK
CIFTALPLVTVVYLLVNISYLTVLTPREILSSDAVAITWADRAFPSLAWIMPFAISTSLF
SNLLISIFKSSRPIYLASQEGQLPLLFNTLNSHSSPFTAVLLLVTLGSLAIILTSLIDLI
NYIFFTGSLWSILLMIGILRRRYQEPNLSIPYKVFLSFPLATIVIDVGLVVIPLVKSPNV
HYVYVLLLVLSGLLFYIPLIHFKIRLAWFEKMTCYLQLLFNICLPDVSEE

Sequence length

470

Interactions

View interactions

SLC7A13 (solute carrier family 7 member 13)