DOCK9

dedicator of cytokinesis 9

Summary

Enables cadherin binding activity. Predicted to be involved in positive regulation of GTPase activity and regulation of Rho protein signal transduction. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants112 total

rsidPosition (GRCh37)AllelesClassClinVar
rs208952841913:99,449,467C/T—uncertain significance
rs77098467013:99,449,475G/A—uncertain significance
rs4127912813:99,449,489G/A—likely benign
rs20192793813:99,452,615C/T—uncertain significance
rs74854359513:99,457,271G/A—uncertain significance
rs20003147313:99,457,286C/T—uncertain significance
rs77116790413:99,457,292C/G—uncertain significance
rs37066502113:99,457,349T/G—uncertain significance
rs254835914713:99,459,942A/T—uncertain significance
rs141825270213:99,459,973T/C—uncertain significance
rs74570709713:99,461,686C/A—uncertain significance
rs6174598713:99,462,473C/T—uncertain significance
rs1161796513:99,476,655G/A—benign
rs254859162713:99,476,711T/G—uncertain significance
rs76267158413:99,476,735C/T—uncertain significance
rs6263759513:99,478,176G/A—uncertain significance
rs120930387913:99,481,572C/T—uncertain significance
rs77645831813:99,481,683G/T—uncertain significance
rs76156407413:99,481,687G/A—likely benign
rs76973913013:99,481,907C/T—uncertain significance
rs57244617913:99,481,935T/C—uncertain significance
rs97937351713:99,481,977C/T—uncertain significance
rs36891140813:99,482,010C/T—uncertain significance
rs77632124613:99,483,756G/A—uncertain significance
rs209276980513:99,483,907T/C—uncertain significance
rs19997967313:99,483,928G/A—uncertain significance
rs254870947313:99,483,952T/A—uncertain significance
rs18262435213:99,489,757C/T—benign
rs75740869213:99,489,776G/A—uncertain significance
rs209337734013:99,498,195G/C—uncertain significance
rs254899846813:99,502,341C/G—uncertain significance
rs75021992213:99,502,364G/C—uncertain significance
rs37202786413:99,505,696C/T—uncertain significance
rs11687779813:99,505,698T/C—uncertain significance
rs254905670213:99,505,736C/G—uncertain significance
rs254909591513:99,508,184T/C—uncertain significance
rs54621171513:99,508,193G/A—uncertain significance
rs86626311613:99,512,773C/T—uncertain significance
rs5588910213:99,515,281C/T—uncertain significance
rs147123638613:99,515,326C/T—uncertain significance
rs254919370613:99,515,631G/C—uncertain significance
rs77942906013:99,515,646A/G—uncertain significance
rs76292473513:99,515,680T/C—uncertain significance
rs37704115813:99,515,704G/A—uncertain significance
rs74932418213:99,515,800G/A—uncertain significance
rs77511707513:99,519,729G/A—uncertain significance
rs37002743813:99,519,759C/T—uncertain significance
rs214207165213:99,519,765A/T—uncertain significance
rs137649437613:99,520,237A/T—uncertain significance
rs124721770213:99,520,243C/T—uncertain significance
rs134498740013:99,520,507T/C—uncertain significance
rs75025424413:99,520,510T/C—uncertain significance
rs122581485213:99,520,514C/T—uncertain significance
rs37654957513:99,520,564A/G—uncertain significance
rs132373845913:99,520,624C/T—uncertain significance
rs37346394813:99,532,159T/C—uncertain significance
rs125158973113:99,532,917T/C—uncertain significance
rs52993726713:99,532,923C/T—uncertain significance
rs254943882313:99,533,825C/T—uncertain significance
rs76267665913:99,533,835T/G—uncertain significance
rs37215294413:99,533,836C/T—likely benign
rs36979526213:99,534,170T/G—uncertain significance
rs37261352713:99,534,173T/C—uncertain significance
rs11653684613:99,534,244T/C—benign
rs36772715513:99,535,333G/A—uncertain significance
rs20122139013:99,535,348T/C—uncertain significance
rs116342001913:99,535,373G/A—uncertain significance
rs76172073813:99,535,380C/A—uncertain significance
rs121095356013:99,536,114G/A—uncertain significance
rs74556433413:99,536,143G/A—uncertain significance
rs20050056613:99,537,338A/C—conflicting classifications of pathogenicity
rs14603813813:99,537,990C/G—likely benign
rs53925913713:99,540,464G/A—uncertain significance
rs37371093713:99,540,753C/T—uncertain significance
rs75452396213:99,549,769A/G—uncertain significance
rs56877078913:99,549,790T/C—uncertain significance
rs129303057713:99,554,048C/T—uncertain significance
rs76264052513:99,554,118A/G—uncertain significance
rs36976795513:99,554,549G/A—uncertain significance
rs77731659013:99,554,550G/C—uncertain significance
rs6262018413:99,554,621G/A—benign
rs14226794313:99,554,629C/T—likely benign
rs86638297813:99,554,730C/T—uncertain significance
rs36775659713:99,555,327A/G—uncertain significance
rs37520793513:99,556,928A/C—uncertain significance
rs76892995713:99,556,939T/G—uncertain significance
rs89430580213:99,567,621G/C—uncertain significance
rs75123240813:99,567,630T/C—uncertain significance
rs76234430613:99,567,679C/A—uncertain significance
rs951351013:99,571,922G/A——
rs951748313:99,572,712A/Gintron variant—
rs135772908613:99,574,316C/G—uncertain significance
rs141192884513:99,575,603G/A—uncertain significance
rs1046726013:99,577,633A/Gintron variant—
rs37574139813:99,578,094G/A—uncertain significance
rs37163926813:99,578,176A/G—likely benign
rs75950570213:99,582,457C/A—uncertain significance
rs77508797313:99,582,462G/A—uncertain significance
rs20147503913:99,582,510G/A—uncertain significance
rs739967913:99,583,736T/Cintron variant—

Showing 100 of 112 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.