CD163L1

CD163 molecule like 1

Summary

This gene encodes a member of the scavenger receptor cysteine-rich (SRCR) superfamily. Members of this family are secreted or membrane-anchored proteins mainly found in cells associated with the immune system. The SRCR family is defined by a 100-110 amino acid SRCR domain, which may mediate protein-protein interaction and ligand binding. The encoded protein contains twelve SRCR domains, a transmembrane region and a cytoplasmic domain. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2014]

Known Variants105 total

rsidPosition (GRCh37)AllelesClassClinVar
rs15038358512:7,483,743C/Adownstream gene variant—
rs18690799312:7,490,950C/Tintergenic variant—
rs55858266212:7,510,047C/T—uncertain significance
rs14775781612:7,514,308G/Aintron variant—
rs76435471212:7,519,835A/G—uncertain significance
rs254048260312:7,519,859C/G—uncertain significance
rs54761038312:7,520,330C/G——
rs14525668512:7,521,535A/G—likely benign
rs194708368512:7,521,541T/C—uncertain significance
rs126593230712:7,521,981G/C—uncertain significance
rs11345478812:7,522,013C/T—uncertain significance
rs37273032412:7,522,052G/A—uncertain significance
rs14284146212:7,522,171G/T—benign
rs254049122412:7,522,189C/T—uncertain significance
rs76941809012:7,522,202C/A—uncertain significance
rs13873312112:7,522,232C/T—uncertain significance
rs37514922612:7,525,989T/C—uncertain significance
rs76329811712:7,525,996A/C—uncertain significance
rs77437991312:7,526,002G/A—uncertain significance
rs14488639712:7,526,063C/T—uncertain significance
rs74543939612:7,526,120T/C—uncertain significance
rs121995081612:7,526,122G/A—uncertain significance
rs74924879212:7,526,147C/T—uncertain significance
rs127999766812:7,527,054T/C—likely benign
rs142305943812:7,527,069C/T—likely benign
rs75089906912:7,527,093G/C—likely benign
rs20054829712:7,527,094C/T—likely benign
rs194721519612:7,527,144A/G—likely benign
rs75932502712:7,527,165C/T—likely benign
rs156577966812:7,527,168C/T—likely benign
rs254050697712:7,527,174A/G—likely benign
rs77507033712:7,527,186G/C—likely benign
rs156577975312:7,527,204C/T—likely benign
rs52852893112:7,527,205A/T—uncertain significance
rs3620671312:7,527,284C/T—likely benign
rs75542491912:7,527,287C/G—uncertain significance
rs144472860712:7,527,310G/A—uncertain significance
rs75727355212:7,527,316C/T—uncertain significance
rs36795202112:7,527,337C/T—uncertain significance
rs76954950512:7,527,487C/T—uncertain significance
rs37385689812:7,527,879G/C—uncertain significance
rs254051117312:7,527,928G/T—uncertain significance
rs76433674312:7,527,937T/C—likely benign
rs14783620912:7,527,996C/G—uncertain significance
rs126271936412:7,527,999A/G—uncertain significance
rs254051160712:7,528,017T/C—uncertain significance
rs13852521712:7,528,192C/Tsplice region variant—
rs15085648712:7,528,404C/Tmissense variant—
rs116997615512:7,528,509A/G—uncertain significance
rs77066218812:7,528,532C/T—uncertain significance
rs76353400112:7,528,533G/A—uncertain significance
rs77512002912:7,528,548G/A—uncertain significance
rs37192075912:7,531,612G/A—uncertain significance
rs14070925112:7,531,685T/C—uncertain significance
rs20215263412:7,531,762C/T—uncertain significance
rs140585259912:7,531,768A/G—uncertain significance
rs137276387612:7,531,770T/G—likely benign
rs103900078112:7,531,775C/A—uncertain significance
rs159189971412:7,531,850A/T—uncertain significance
rs119915820012:7,531,862C/T—uncertain significance
rs14079910512:7,531,882A/G—uncertain significance
rs7852453412:7,535,882C/Tintron variant—
rs748519412:7,539,260T/A——
rs1230084312:7,542,724C/Tintron variant—
rs194776953112:7,548,786C/T—uncertain significance
rs14541178312:7,548,969C/A—likely benign
rs407279612:7,548,996C/Amissense variant—
rs75756507412:7,549,006C/T—uncertain significance
rs407510612:7,550,186G/T——
rs14073083912:7,550,868G/A—likely benign
rs75101021112:7,550,893C/T—likely benign
rs37442542412:7,550,913C/A—uncertain significance
rs37457716212:7,550,952A/G—uncertain significance
rs102003390812:7,550,959A/G—uncertain significance
rs77397767212:7,550,977T/C—uncertain significance
rs1230592012:7,553,051G/Tintron variant—
rs7519603212:7,554,386A/Tintron variant—
rs413130512:7,555,416G/Cintron variant—
rs14668464812:7,556,160C/T—uncertain significance
rs77229516912:7,556,212A/T—uncertain significance
rs77941610512:7,556,281G/A—uncertain significance
rs37127762812:7,556,316T/C—uncertain significance
rs98403656512:7,559,167C/A—uncertain significance
rs77100319912:7,559,172T/C—uncertain significance
rs146653953212:7,559,260A/T—uncertain significance
rs76142768512:7,559,309C/G—uncertain significance
rs75821788512:7,559,393T/A—uncertain significance
rs8019086312:7,559,397C/T—uncertain significance
rs37445193112:7,559,401T/C—likely benign
rs7650253512:7,560,468C/Tintron variant—
rs54462307912:7,568,629C/A——
rs7946143112:7,571,500A/Gintron variant—
rs796560712:7,574,652T/Gintron variant—
rs797375212:7,574,821G/Aintron variant—
rs77060000512:7,585,135G/T—uncertain significance
rs74530910012:7,585,137A/C—uncertain significance
rs37116734212:7,585,293T/G—uncertain significance
rs76607145112:7,586,021A/G—uncertain significance
rs130492433312:7,586,026C/T—uncertain significance
rs14254117912:7,586,047G/C—uncertain significance

Showing 100 of 105 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.