centrosomal protein 152

Summary
Gene Symbol
  • CEP152
Organism
Homo sapiens (human)
NCBI Gene
22995
PubChem
22995
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Cilium biogenesis/degradation
  • Coiled coil
  • Cytoskeleton
  • Disease variant
  • Dwarfism
  • Intellectual disability
  • Phosphoprotein
  • Primary microcephaly
  • Reference proteome
Proteins
Displaying all 2 entries
UniProt Protein Name
O94986
Q3B7A2
Gene Ontology (GO)
Disease
Disease Ontology
Displaying all 2 entries
DO ID Disease Name Source
DOID:0070012 Seckel syndrome 5
DOID:0070292 primary autosomal recessive microcephaly 9

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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: August 4, 2025