prominin 1

Summary
Gene Symbol
  • PROM1
Organism
Homo sapiens (human)
NCBI Gene
8842
PubChem
8842
Alliance of Genome Resources
Annotation
Keyword
  • Acetylation
  • Alternative splicing
  • Cell membrane
  • Cilium
  • Coiled coil
  • Cone-rod dystrophy
  • Direct protein sequencing
  • Disease variant
  • Endoplasmic reticulum
  • Glycoprotein
  • Phosphoprotein
  • Reference proteome
  • Retinitis pigmentosa
  • Signal
  • Stargardt disease
  • Transmembrane helix
Proteins
Displaying all 2 entries
UniProt Protein Name
A0A0A0N0M1
O43490
  • Antigen AC133
  • Prominin-like protein 1
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Prominin
Functional Category
  • P: Inorganic ion transport and metabolism
  • T: Signal transduction mechanisms
Displaying 1 entry
Gene Ontology
cholesterol binding
Displaying 1 entry
InterPro
Prominin
Disease
Disease Ontology
Displaying all 5 entries
DO ID Disease Name Source
DOID:0070517 retinal macular dystrophy 2
DOID:0110376 retinitis pigmentosa 41
DOID:0111019 cone-rod dystrophy 12
DOID:8466 retinal degeneration
DOID:9351 diabetes mellitus

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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


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Last updated: December 9, 2024