SLC6A15 (solute carrier family 6 member 15)
Gene | |
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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55117 |
Gene name
Gene Name - the full gene name approved by the HGNC.
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Solute carrier family 6 member 15 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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SLC6A15 |
Synonyms (NCBI Gene)
Gene synonyms aliases
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NTT73, SBAT1, V7-3, hv7-3 |
Chromosome
Chromosome number
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12 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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12q21.31 |
Summary
Summary of gene provided in NCBI Entrez Gene.
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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.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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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
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Tissue specificity | TISSUE SPECIFICITY: Almost exclusively expressed in the brain. {ECO:0000269|PubMed:16226721}. | ||||||||||
Sequence |
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Sequence length | 730 | ||||||||||
Interactions | View interactions |
Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease information provided by ClinVar, GenCC, and GWAS databases.
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