Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55117
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 6 member 15
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC6A15
Synonyms (NCBI Gene) Gene synonyms aliases
NTT73, SBAT1, V7-3, hv7-3
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q21.31
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the solute carrier family 6 protein family which transports neutral amino acids. The encoded protein is thought to play a role in neuronal amino acid transport (PMID: 16185194) and may be associated with major depression (PMI
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT050428 hsa-miR-23a-3p CLASH 23622248
MIRT046356 hsa-miR-23b-3p CLASH 23622248
MIRT042665 hsa-miR-196b-5p CLASH 23622248
MIRT1366058 hsa-miR-101 CLIP-seq
MIRT1366059 hsa-miR-1244 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003333 Process Amino acid transmembrane transport IEA
GO:0005295 Function Neutral L-amino acid:sodium symporter activity IDA 16226721
GO:0005295 Function Neutral L-amino acid:sodium symporter activity IEA
GO:0005298 Function Proline:sodium symporter activity IBA
GO:0005298 Function Proline:sodium symporter activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607971 13621 ENSG00000072041
Protein
UniProt ID Q9H2J7
Protein name Sodium-dependent neutral amino acid transporter B(0)AT2 (Sodium- and chloride-dependent neurotransmitter transporter NTT73) (Sodium-coupled branched-chain amino-acid transporter 1) (Solute carrier family 6 member 15) (Transporter v7-3)
Protein function Functions as a sodium-dependent neutral amino acid transporter. Exhibits preference for the branched-chain amino acids, particularly leucine, valine and isoleucine and methionine. Can also transport low-affinity substrates such as alanine, pheny
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00209 SNF 61 644 Sodium:neurotransmitter symporter family Family
Tissue specificity TISSUE SPECIFICITY: Almost exclusively expressed in the brain. {ECO:0000269|PubMed:16226721}.
Sequence
Sequence length 730
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Amino acid transport across the plasma membrane
Na+/Cl- dependent neurotransmitter transporters
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Breast Cancer Breast cancer N/A N/A GWAS
Colorectal Cancer ICD10 C18, C19, C20: colorectal cancer N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS
Gastroesophageal Reflux Disease Gastroesophageal reflux disease N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Colonic Neoplasms Associate 37543674
Colorectal Neoplasms Associate 21298349, 24485021
Depressive Disorder Major Associate 23874702
Insulin Resistance Associate 30913280
Leukemia Large Granular Lymphocytic Associate 35015834
Mental Disorders Associate 23874702
Metabolic Syndrome Associate 30913280
Neoplasms Inhibit 35659616
Neoplasms Associate 37543674
Ovarian Neoplasms Inhibit 28793334