coiled-coil and C2 domain containing 2A

Summary
Gene Symbol
  • CC2D2A
Organism
Homo sapiens (human)
NCBI Gene
57545
PubChem
57545
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Cilium
  • Cilium biogenesis/degradation
  • Coiled coil
  • Cytoskeleton
  • Disease variant
  • Joubert syndrome
  • Meckel syndrome
  • Reference proteome
  • Retinitis pigmentosa
Proteins
Displaying 1 entry
UniProt Protein Name
Q9P2K1
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
C2 domain-containing protein
Functional Category
  • O: Posttranslational modification, protein turnover, chaperones
  • P: Inorganic ion transport and metabolism
  • T: Signal transduction mechanisms
Displaying 1 entry
Gene Ontology
protein localization to ciliary transition zone
Displaying all 2 entries
InterPro
C2 domain superfamily
CC2D2A, N-terminal, C2 domain
Disease
Disease Ontology
Displaying all 8 entries
DO ID Disease Name Source
DOID:0050545 visceral heterotaxy
DOID:0050777 Joubert syndrome
DOID:0050778 Meckel syndrome
DOID:0060340 ciliopathy
DOID:0070120 Meckel syndrome 6
DOID:0111004 Joubert syndrome 9
DOID:10584 retinitis pigmentosa
DOID:1059 intellectual disability

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International Collaboration

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