solute carrier family 17 member 8

Summary
Gene Symbol
  • SLC17A8
Organism
Homo sapiens (human)
NCBI Gene
246213
PubChem
246213
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Cell membrane
  • Chloride channel
  • Cytoplasmic vesicle
  • Disease variant
  • Glycoprotein
  • Hearing
  • Neurotransmitter transport
  • Non-syndromic deafness
  • Phosphate transport
  • Reference proteome
  • Sodium transport
  • Symport
  • Synaptosome
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
Q8NDX2
  • Solute carrier family 17 member 8
Gene Ontology (GO)
GO Hierarchy
Displaying entries 1 - 5 of 12 in total
GO Term Evidence Code PMID
glial limiting end-foot
axon terminus
synaptic vesicle membrane
multivesicular body
basal dendrite
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
transporter
Functional Category
  • C: Energy production and conversion
  • E: Amino acid transport and metabolism
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 8 entries
DO ID Disease Name Source
DOID:0080855 Parkinsonism
DOID:0110555 autosomal dominant nonsyndromic deafness 25
DOID:11446 sciatic neuropathy
DOID:1289 neurodegenerative disease
DOID:14330 Parkinson's disease
DOID:224 transient cerebral ischemia
DOID:5463 cochlear disease
DOID:9784 trichinosis

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024