KIZ

kizuna centrosomal protein

Summary

The protein encoded by this gene localizes to centrosomes, strengthening and stabilizing the pericentriolar region prior to spindle formation. The encoded protein usually remains with the mother centrosome after centrosomal duplication. Sevral transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2013]

Known Variants383 total

rsidPosition (GRCh37)AllelesClassClinVar
rs141422532020:21,106,691C/G—uncertain significance
rs147383578620:21,106,704C/T—uncertain significance
rs36879620820:21,106,738C/T—likely benign
rs143813453320:21,106,759G/A—pathogenic
rs203144138020:21,106,763C/T—uncertain significance
rs251955528420:21,106,765G/A—likely benign
rs90763030320:21,106,767C/T—uncertain significance
rs135129015720:21,106,769C/T—uncertain significance
rs37344145120:21,106,770T/G—uncertain significance
rs203144285720:21,106,771C/G—likely benign
rs55576176620:21,106,772G/T—uncertain significance
rs77293708220:21,106,780C/G—likely benign
rs74702129120:21,106,783G/T—likely benign
rs97530462120:21,106,786C/A—uncertain significance
rs251955586420:21,106,788T/A—uncertain significance
rs77098937620:21,106,791C/A—pathogenic
rs138138337120:21,106,792G/C—likely benign
rs15024316820:21,106,804C/T—likely benign
rs58777737620:21,106,808G/Tcoding sequence variantpathogenic
rs124392199520:21,106,812G/C—uncertain significance
rs98840819720:21,106,820C/T—pathogenic
rs92163647320:21,106,831C/T—likely benign
rs54155590920:21,106,851G/A—uncertain significance
rs251955729920:21,106,854A/C—likely benign
rs251955742620:21,106,863G/A—likely benign
rs117557130320:21,112,722A/C—likely benign
rs104371256320:21,112,724G/A—likely benign
rs37301806620:21,112,734A/G—likely benign
rs203188513020:21,112,735T/C—uncertain significance
rs212230991220:21,112,741A/G—likely benign
rs74995153020:21,112,750A/T—uncertain significance
rs134468615220:21,112,756C/T—likely benign
rs119910291120:21,112,758T/C—uncertain significance
rs212231049720:21,112,764A/G—uncertain significance
rs212231053420:21,112,765G/T—likely pathogenic
rs251959758420:21,112,766A/G—uncertain significance
rs58777737720:21,112,767——pathogenic
rs251959772520:21,112,778T/C—uncertain significance
rs212231079920:21,112,779A/G—uncertain significance
rs37233053520:21,112,790G/C—likely benign
rs251959799620:21,112,791A/G—uncertain significance
rs11610012920:21,112,810G/A—likely benign
rs203189156020:21,112,818G/A—likely benign
rs129648505920:21,112,820A/G—likely benign
rs55320167020:21,117,011A/T—likely benign
rs37452499720:21,117,020T/A—likely benign
rs251962374920:21,117,021A/G—likely benign
rs135855766920:21,117,029A/G—likely pathogenic
rs212237157120:21,117,034T/G—likely benign
rs131946373620:21,117,056A/G—uncertain significance
rs251962421220:21,117,071G/A—uncertain significance
rs136426105820:21,117,077T/G—uncertain significance
rs251962433120:21,117,081A/G—uncertain significance
rs203219267020:21,117,086G/A—uncertain significance
rs77000899720:21,117,095G/T—uncertain significance
rs251962442320:21,117,097T/C—likely benign
rs93033742220:21,117,099A/G—uncertain significance
rs20221081920:21,117,104C/Tcoding sequence variantpathogenic
rs98237396820:21,117,105G/A—uncertain significance
rs251962465120:21,117,111A/C—uncertain significance
rs74902567520:21,117,114A/G—uncertain significance
rs203219503920:21,117,125C/T—pathogenic
rs212237329820:21,117,131G/C—uncertain significance
rs19993746420:21,117,134C/T—likely benign
rs37380309520:21,117,135G/A—conflicting classifications of pathogenicity
rs251962497020:21,117,137G/C—uncertain significance
rs76600254520:21,117,152G/C—uncertain significance
rs75924116220:21,117,154A/C—uncertain significance
rs90163611320:21,117,155C/T—uncertain significance
rs132051733720:21,117,160C/T—likely benign
rs36797044320:21,117,162C/T—uncertain significance
rs142204675720:21,117,198C/A—uncertain significance
rs251962573420:21,117,201C/T—likely benign
rs78157051720:21,117,210T/C—likely benign
rs74798975320:21,126,188A/G—likely benign
rs604727120:21,126,194C/G—benign
rs119004130320:21,126,204A/G—likely pathogenic
rs147755390420:21,126,208C/T—conflicting classifications of pathogenicity
rs20086016620:21,126,209G/A—uncertain significance
rs167073972520:21,126,233A/G—uncertain significance
rs124462254120:21,126,235G/A—uncertain significance
rs1698251320:21,126,238A/T—likely benign
rs131405935920:21,126,247A/C—uncertain significance
rs77781263320:21,126,249A/T—uncertain significance
rs126796040920:21,126,252G/A—uncertain significance
rs251967965820:21,126,272C/A—uncertain significance
rs203280736220:21,126,273T/G—uncertain significance
rs18956511020:21,126,276C/T—uncertain significance
rs57097851820:21,126,286C/G—uncertain significance
rs144324167320:21,126,300T/C—uncertain significance
rs37255643720:21,126,305T/C—likely benign
rs147584456520:21,126,308A/G—likely benign
rs119085678020:21,126,309T/C—likely benign
rs122108927620:21,126,313T/C—likely benign
rs117986911420:21,126,314A/G—likely benign
rs603579020:21,135,597G/A——
rs203367612020:21,142,518G/A—uncertain significance
rs481502520:21,142,523C/T—likely benign
rs37005179220:21,142,525A/C—conflicting classifications of pathogenicity
rs160041578320:21,142,532T/C—likely benign

Showing 100 of 383 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.