SPNS lysolipid transporter 2, sphingosine-1-phosphate

Summary
Gene Symbol
  • SPNS2
Organism
Homo sapiens (human)
NCBI Gene
124976
PubChem
124976
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Cell membrane
  • Disease variant
  • Endosome
  • Lipid transport
  • Non-syndromic deafness
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
Q8IVW8
  • Protein spinster homolog 2
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
transporter
Functional Category
  • E: Amino acid transport and metabolism
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 3 entries
DO ID Disease Name Source
DOID:0111643 autosomal recessive nonsyndromic deafness 115
DOID:14503 neuronal ceroid lipofuscinosis
DOID:1927 sphingolipidosis

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024