cochlin

Summary
Gene Symbol
  • COCH
Organism
Homo sapiens (human)
NCBI Gene
1690
PubChem
1690
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Disease variant
  • Disulfide bond
  • Extracellular matrix
  • Glycoprotein
  • Hearing
  • Non-syndromic deafness
  • Proteomics identification
  • Reference proteome
  • Repeat
  • Signal
Proteins
Displaying all 2 entries
UniProt Protein Name
O43405
  • COCH-5B2
A0A2U3TZE7
OrthoDB (Group)
Group level
Eukaryota
Group Name
c-type lectin
Functional Category
  • M: Cell wall/membrane/envelope biogenesis
  • Q: Secondary metabolites biosynthesis, transport and catabolism
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying all 2 entries
DO ID Disease Name Source
DOID:0110593 autosomal dominant nonsyndromic deafness 9
DOID:0111644 autosomal recessive nonsyndromic deafness 110

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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: April 7, 2025