CEP97 (centrosomal protein 97)

2014-11-01  

Identity

HGNC
LOCATION
3q12.3
LOCUSID
ALIAS
2810403B08Rik,LRRIQ2

Other Information

Locus ID:

NCBI: 79598
MIM: 615864
HGNC: 26244
Ensembl: ENSG00000182504

Variants:

dbSNP: 79598
ClinVar: 79598
TCGA: ENSG00000182504
COSMIC: CEP97

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000182504ENST00000341893Q8IW35
ENSG00000182504ENST00000465011F8WF91
ENSG00000182504ENST00000467655H7C4Y5
ENSG00000182504ENST00000494050E9PG22

Expression (GTEx)

0
5
10
15

Pathways

PathwaySourceExternal ID
Organelle biogenesis and maintenanceREACTOMER-HSA-1852241
Cilium AssemblyREACTOMER-HSA-5617833
Anchoring of the basal body to the plasma membraneREACTOMER-HSA-5620912

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
304048372018Cullin-3-KCTD10-mediated CEP97 degradation promotes primary cilium formation.1

Citation

Dessen P

CEP97 (centrosomal protein 97)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/61735/cep97