claudin 9

Summary
Gene Symbol
  • CLDN9
Organism
Homo sapiens (human)
NCBI Gene
9080
PubChem
9080
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Cell membrane
  • Host cell receptor for virus entry
  • Host-virus interaction
  • Non-syndromic deafness
  • Reference proteome
  • Tight junction
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
O95484
Gene Ontology (GO)
OrthoDB (Group)
Group level
Eukaryota
Group Name
claudin i
Functional Category
  • M: Cell wall/membrane/envelope biogenesis
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Displaying all 2 entries
Gene Ontology
bicellular tight junction assembly
structural molecule activity
Displaying all 3 entries
InterPro
Claudin, conserved site
Claudin
PMP-22/EMP/MP20/Claudin
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0112162 autosomal recessive nonsyndromic deafness 116

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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