Homo sapiens Gene: SLC6A17
Summary
InnateDB Gene IDBG-100956.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC6A17
Gene Name solute carrier family 6, member 17
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000197106
Encoded Proteins
solute carrier family 6, member 17
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The SLC6 family of proteins, which includes SLC6A17, acts as specific transporters for neurotransmitters, amino acids, and osmolytes like betaine, taurine, and creatine. SLC6 proteins are sodium cotransporters that derive the energy for solute transport from the electrochemical gradient for sodium ions (Hoglund et al., 2005 [PubMed 16125675]).[supplied by OMIM, Mar 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 1:110150486-110202202
Strand Forward strand
Band p13.3
Transcripts
ENST00000331565 ENSP00000330199
ENST00000465159
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005328 neurotransmitter:sodium symporter activity
Biological Process
GO:0006836 neurotransmitter transport
GO:0015804 neutral amino acid transport
GO:0015816 glycine transport
GO:0015820 leucine transport
GO:0015824 proline transport
GO:0032328 alanine transport
GO:0055085 transmembrane transport
Cellular Component
GO:0005887 integral component of plasma membrane
GO:0008021 synaptic vesicle
GO:0016021 integral component of membrane
GO:0030054 cell junction
GO:0030672 synaptic vesicle membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
Non-SSD Ortholog
Possible paralog/unusual divergence/ gene prediction error
Not yet available
Non-SSD Ortholog
Possible paralog/unusual divergence/ gene prediction error
Cross-References
SwissProt Q9H1V8
TrEMBL
UniProt Splice Variant
Entrez Gene 388662
UniGene Hs.128382
RefSeq NM_001010898 XM_006710643
HUGO HGNC:31399
OMIM 610299
CCDS CCDS30799
HPRD
IMGT
EMBL AK289982 AL137790 AL355990 BC140908
GenPept AAI40909 BAF82671 CAI18832 CAI18927
RNA Seq Atlas 388662