| CEP162 |
| LOCUS ID | 22832 | ||||||||||
| GENE_SYMBOL | CEP162 | ||||||||||
| GENE NAME | centrosomal protein | ||||||||||
| SYNONYMNS | QN1, C6orf84, KIAA1009 | ||||||||||
| CHROMOSOME | 6 | ||||||||||
| HOMOLOGENE ID | 8930 |
| microRNAs | NA | NA |
| 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 |
| Retinopathy | 1. Moreover, association between the ciliary gene CEP162 and DR was established in terms of retinal neural processing, confirming previous reports. | 31130920 |