CNPPD1

cyclin Pas1/PHO80 domain containing 1

Summary

Predicted to enable cyclin-dependent protein serine/threonine kinase regulator activity. Predicted to be located in membrane. Predicted to be part of cyclin-dependent protein kinase holoenzyme complex. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants34 total

rsidPosition (GRCh37)AllelesClassClinVar
rs64361222:220,036,390A/Gregulatory region variant—
rs24697162532:220,037,385G/A—uncertain significance
rs7603647432:220,037,417G/T—uncertain significance
rs24697165022:220,037,423A/T—uncertain significance
rs7727610192:220,037,429T/C—uncertain significance
rs115525802:220,037,479G/C—uncertain significance
rs11929155442:220,037,550T/C—uncertain significance
rs7679772112:220,037,634T/A—uncertain significance
rs1488630972:220,037,675A/G—uncertain significance
rs3700405372:220,037,741G/A—uncertain significance
rs10431602:220,037,756A/Gmissense variant—
rs7668424052:220,037,804G/A—uncertain significance
rs3710881922:220,037,834G/A—uncertain significance
rs3683822732:220,038,118G/A—uncertain significance
rs7567432792:220,038,145G/A—uncertain significance
rs1410603322:220,038,170G/A—uncertain significance
rs11922330172:220,038,890C/T—uncertain significance
rs3681393522:220,038,905G/A—uncertain significance
rs7671585812:220,039,532T/C—uncertain significance
rs24697242452:220,039,547C/T—uncertain significance
rs7575271142:220,039,561G/A—uncertain significance
rs7587674492:220,039,598C/T—uncertain significance
rs7468042742:220,039,718T/C—uncertain significance
rs24697250502:220,039,732G/C—uncertain significance
rs2000524712:220,040,314G/A—uncertain significance
rs14162034372:220,040,336C/A—uncertain significance
rs12735263112:220,040,353T/C—uncertain significance
rs7738899082:220,040,371T/C—uncertain significance
rs14164575032:220,040,973G/C—uncertain significance
rs3748473652:220,040,974C/T—uncertain significance
rs3691687862:220,040,983G/A—uncertain significance
rs64361242:220,041,433C/T——
rs1503424792:220,041,538C/T—uncertain significance
rs1408196682:220,041,654C/Gregulatory region variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.