SDK2

sidekick cell adhesion molecule 2

Summary

The protein encoded by this gene is a member of the immunoglobulin superfamily. The protein contains two immunoglobulin domains and thirteen fibronectin type III domains. Fibronectin type III domains are present in both extracellular and intracellular proteins and tandem repeats are known to contain binding sites for DNA, heparin and the cell surface. This protein, and a homologous mouse sequence, are very similar to the Drosophila sidekick gene product but the specific function of this superfamily member is not yet known. Evidence for alternative splicing at this gene locus has been observed but the full-length nature of additional variants has not yet been determined. [provided by RefSeq, Jul 2008]

Known Variants224 total

rsidPosition (GRCh37)AllelesClassClinVar
rs37159952917:71,334,751A/G—uncertain significance
rs14723603117:71,334,790C/T—likely benign
rs75723125217:71,334,791G/A—uncertain significance
rs75233457117:71,334,836G/T—uncertain significance
rs14445288517:71,334,862C/T—uncertain significance
rs77801478217:71,334,869G/C—uncertain significance
rs98209276017:71,334,873G/T—likely benign
rs77796341317:71,334,944T/G—uncertain significance
rs74951589417:71,334,958C/G—uncertain significance
rs381699517:71,335,260G/Aintron variant—
rs37411763117:71,344,733C/G—likely benign
rs54701099317:71,344,789A/G—likely benign
rs75360992417:71,344,800C/T—uncertain significance
rs37602025117:71,344,822A/C—uncertain significance
rs77460210417:71,346,379G/T—uncertain significance
rs37531636917:71,346,416C/T—uncertain significance
rs13800341917:71,346,417G/A—likely benign
rs13948013517:71,346,479C/T—uncertain significance
rs77377794417:71,346,480G/T—uncertain significance
rs3531792517:71,346,513C/T—benign
rs75711330117:71,346,794T/A—uncertain significance
rs251126507017:71,346,820C/G—uncertain significance
rs37052061117:71,346,921C/T—uncertain significance
rs54068071017:71,348,618C/T—uncertain significance
rs37371549917:71,348,646G/A—likely benign
rs101991450117:71,348,749T/A—uncertain significance
rs76247801617:71,354,307C/T—uncertain significance
rs76610101817:71,354,308G/A—uncertain significance
rs13852776517:71,357,828C/T—uncertain significance
rs54119991617:71,357,829C/T—uncertain significance
rs77049143117:71,357,832G/C—uncertain significance
rs75651026217:71,357,868A/G—uncertain significance
rs99306754517:71,357,891C/T—uncertain significance
rs54183661817:71,357,915G/A—uncertain significance
rs14342060117:71,357,958C/T—uncertain significance
rs14798354317:71,357,964C/T—uncertain significance
rs13880275717:71,361,436C/T—uncertain significance
rs13953564617:71,364,577G/A—likely benign
rs77122042217:71,364,602T/C—uncertain significance
rs77488504317:71,364,609C/T—uncertain significance
rs75825546317:71,364,632G/A—uncertain significance
rs77808984617:71,364,661G/C—uncertain significance
rs77598080617:71,364,692C/T—uncertain significance
rs251131166217:71,375,359G/A—uncertain significance
rs77894551017:71,375,373G/A—likely benign
rs13938874217:71,375,388C/T—likely benign
rs78037273817:71,375,393C/T—uncertain significance
rs77212425517:71,375,599C/T—uncertain significance
rs7814505617:71,375,642G/A—benign
rs77866034317:71,375,650C/T—uncertain significance
rs77533527017:71,375,658C/T—uncertain significance
rs14132807417:71,375,666G/A—likely benign
rs37314653117:71,375,674T/C—uncertain significance
rs18396264617:71,375,693G/T—likely benign
rs77769319017:71,377,062C/T—uncertain significance
rs76437601817:71,377,074C/A—uncertain significance
rs37091277917:71,377,075G/A—uncertain significance
rs206282557517:71,377,092A/T—likely benign
rs77343521917:71,380,096G/A—uncertain significance
rs37763957117:71,380,099A/G—uncertain significance
rs19963030817:71,380,108G/A—uncertain significance
rs76386931217:71,380,149G/A—uncertain significance
rs37001531917:71,381,997T/C—uncertain significance
rs56261129517:71,382,003C/T—uncertain significance
rs11729134217:71,382,022C/T—benign
rs53363828917:71,382,027C/T—uncertain significance
rs7818598417:71,382,049A/G—benign
rs75066960117:71,382,643T/C—uncertain significance
rs37189439617:71,382,672C/T—likely benign
rs77075786117:71,382,687C/A—uncertain significance
rs74886465117:71,383,979C/T—uncertain significance
rs77843858817:71,383,985T/C—likely benign
rs11550223017:71,383,998A/G—benign
rs36992839117:71,384,009C/T—uncertain significance
rs227072417:71,384,080G/C—benign
rs20024232317:71,384,097T/C—benign
rs14909378517:71,384,117C/T—uncertain significance
rs78036902917:71,384,120T/G—uncertain significance
rs55880435317:71,384,123G/A—uncertain significance
rs14738484017:71,384,151C/T—likely benign
rs13952742717:71,384,169T/C—benign
rs75384819317:71,386,453C/G—uncertain significance
rs77148402917:71,386,480G/A—uncertain significance
rs251133127917:71,386,488G/C—uncertain significance
rs37125779917:71,386,547G/T—benign
rs3528908817:71,387,632G/A—uncertain significance
rs137777932917:71,387,662A/C—uncertain significance
rs74906311917:71,387,681G/C—likely benign
rs20209637817:71,389,690C/T—likely benign
rs77338693017:71,389,710G/A—uncertain significance
rs76808828817:71,389,734C/T—uncertain significance
rs206294734417:71,389,798C/T—uncertain significance
rs20098240017:71,389,804C/T—uncertain significance
rs18153372217:71,389,821C/Tmissense variant—
rs75807268517:71,389,832G/T—likely benign
rs37674630917:71,390,373C/T—uncertain significance
rs75859771217:71,390,400C/T—uncertain significance
rs124169310417:71,390,404C/T—uncertain significance
rs206295282317:71,390,418G/C—uncertain significance
rs14082418917:71,391,302C/T—uncertain significance

Showing 100 of 224 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.