transmembrane protein 63C

Summary
Gene Symbol
  • TMEM63C
Organism
Homo sapiens (human)
NCBI Gene
57156
PubChem
57156
Alliance of Genome Resources
Annotation
Keyword
  • Calcium
  • Cell membrane
  • Disease variant
  • Endoplasmic reticulum
  • Hereditary spastic paraplegia
  • Ion channel
  • Phosphoprotein
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
Q9P1W3
  • Transmembrane protein 63C
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
CSC1-like protein
Functional Category
  • E: Amino acid transport and metabolism
  • G: Carbohydrate transport and metabolism
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 3 entries
DO ID Disease Name Source
DOID:0070456 hereditary spastic paraplegia 87
DOID:1312 focal segmental glomerulosclerosis
DOID:331 central nervous system disease

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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