clarin 2

Summary
Gene Symbol
  • CLRN2
Organism
Homo sapiens (human)
NCBI Gene
645104
PubChem
645104
Alliance of Genome Resources
Annotation
Keyword
  • Cell membrane
  • Cell projection
  • Disease variant
  • Glycoprotein
  • Hearing
  • Non-syndromic deafness
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
A0PK11
Gene Ontology (GO)
Displaying 1 entry
GO Term Evidence Code PMID
protein binding
OrthoDB (Group)
Group level
Eukaryota
Group Name
Uncharacterized protein
Functional Category
  • M: Cell wall/membrane/envelope biogenesis
  • Q: Secondary metabolites biosynthesis, transport and catabolism
  • T: Signal transduction mechanisms
Displaying 1 entry
Gene Ontology
sensory perception of sound
Displaying 1 entry
InterPro
Clarin
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0050565 autosomal recessive nonsyndromic deafness

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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