Homo sapiens Gene: SLC17A6
Summary
InnateDB Gene IDBG-36152.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC17A6
Gene Name solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000091664
Encoded Proteins
solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Currently no Entrez Summary Available. You might want to check the Summary Sections of the Orthologs.
Gene Information
Type Protein coding
Genomic Location Chromosome 11:22338097-22379503
Strand Forward strand
Band p14.3
Transcripts
ENST00000263160 ENSP00000263160
ENST00000534115
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 3 interaction(s) predicted by orthology.
Predicted by orthology
Total 3 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005313 L-glutamate transmembrane transporter activity
GO:0015293 symporter activity
Biological Process
GO:0001504 neurotransmitter uptake
GO:0006811 ion transport
GO:0006814 sodium ion transport
GO:0015813 L-glutamate transport
GO:0055085 transmembrane transport
Cellular Component
GO:0008021 synaptic vesicle
GO:0016021 integral component of membrane
GO:0030054 cell junction
GO:0030672 synaptic vesicle membrane
GO:0043005 neuron projection
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Pathways
NETPATH
REACTOME
Transmembrane transport of small molecules pathway
Transport of inorganic cations/anions and amino acids/oligopeptides pathway
Organic anion transporters pathway
SLC-mediated transmembrane transport pathway
KEGG
INOH
PID BIOCARTA
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.242821
RefSeq NM_020346
HUGO
OMIM
CCDS CCDS7856
HPRD 10459
IMGT
EMBL
GenPept
RNA Seq Atlas