CEP162
LOCUS ID22832
GENE_SYMBOLCEP162
GENE NAMEcentrosomal protein
SYNONYMNSQN1, C6orf84, KIAA1009
CHROMOSOME6
HOMOLOGENE ID8930
microRNAsNANA
GENE SUMMARY
CEP162 (Centrosomal Protein 162) is a Protein Coding gene. Diseases associated with CEP162 include Seckel Syndrome 7 and Orofaciodigital Syndrome Ix. Among its related pathways are Organelle biogenesis and maintenance and Regulation of PLK1 Activity at G2/M Transition.

OBSERVATIONS

Complication Evidence PMID
Retinopathy1. Moreover, association between the ciliary gene CEP162 and DR was established in terms of retinal neural processing, confirming previous reports. 31130920