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Gene: SLC17A8 (solute carrier family 17 member 8) 
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Symbol: SLC17A8
Name: solute carrier family 17 member 8
Description: INVOLVED IN L-glutamate transmembrane transport (inferred); PARTICIPATES IN auditory mechanotransduction pathway; glutamate signaling pathway; ASSOCIATED WITH autosomal dominant nonsyndromic deafness 25 (ortholog); cochlear disease (ortholog); Hyperalgesia (ortholog); FOUND IN integral component of plasma membrane (inferred)
Type: protein-coding
RefSeq Status: MODEL
Also known as: LOW QUALITY PROTEIN: vesicular glutamate transporter 3; solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8; solute carrier family 17 (vesicular glutamate transporter), member 8
Orthologs:
Latest Assembly: Sscrofa11.1 - Pig Sscrofa11.1 Assembly
Position:
AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1583,741,641 - 83,809,472 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2587,686,292 - 87,696,625 (+)NCBISscrofa10.2Sscrofa10.2susScr3
Pig Cytomap5 NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model



Genomics

Comparative Map Data

Expression


Sequence

Nucleotide Sequences
Protein Sequences

Additional Information

External Database Links
 
More on SLC17A8
NCBI Gene
Ensembl Gene
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 14171251
Created: 2019-01-29
Species:
Last Modified: 2019-10-16
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.