SSC5D

scavenger receptor cysteine rich family member with 5 domains

Summary

Predicted to enable fibronectin binding activity; laminin binding activity; and scavenger receptor activity. Predicted to be involved in defense response; detection of bacterial lipoprotein; and negative regulation of interleukin-8 production. Predicted to act upstream of or within regulation of interleukin-8 production. Predicted to be located in collagen-containing extracellular matrix. Predicted to be active in extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Apr 2025]

Known Variants180 total

rsidPosition (GRCh37)AllelesClassClinVar
rs5579952319:55,999,545C/Aregulatory region variant
rs100009418819:56,000,744C/Tuncertain significance
rs95566944319:56,000,756G/Auncertain significance
rs53591073419:56,000,762C/Tuncertain significance
rs74628091319:56,000,765C/Guncertain significance
rs77156207319:56,000,786C/Tuncertain significance
rs119861154119:56,000,822C/Tuncertain significance
rs104489301219:56,000,828G/Auncertain significance
rs55892356419:56,000,852G/Auncertain significance
rs78177406519:56,000,858G/Auncertain significance
rs101859312219:56,000,877C/Tuncertain significance
rs77282993219:56,000,885G/Auncertain significance
rs75613670819:56,000,937G/Auncertain significance
rs147864604819:56,000,939G/Cuncertain significance
rs57490007719:56,000,972C/Tuncertain significance
rs142365768119:56,000,973G/Auncertain significance
rs75671342319:56,001,011G/Auncertain significance
rs20169587319:56,001,026G/Auncertain significance
rs20115127319:56,001,275G/Cuncertain significance
rs90874848219:56,001,294A/Guncertain significance
rs142609818719:56,001,330G/Tuncertain significance
rs145708850619:56,001,333C/Guncertain significance
rs56085582419:56,001,670C/Tlikely benign
rs52997542019:56,001,671G/Auncertain significance
rs198710153619:56,001,689A/Guncertain significance
rs37736118019:56,001,693C/Tlikely benign
rs105501123219:56,001,700C/Tuncertain significance
rs53871066819:56,001,701G/Auncertain significance
rs92307516319:56,001,716G/Auncertain significance
rs251425570419:56,001,737C/Tuncertain significance
rs88846768819:56,001,745C/Auncertain significance
rs74873767119:56,001,755C/Auncertain significance
rs103742998819:56,002,147C/Tuncertain significance
rs76082204719:56,002,167C/Auncertain significance
rs75959697419:56,002,176C/Tlikely benign
rs119996298019:56,002,177G/Auncertain significance
rs53148151119:56,002,192T/Cuncertain significance
rs54877817219:56,002,205G/Auncertain significance
rs75451061819:56,002,225G/Auncertain significance
rs142281721819:56,002,242C/Tlikely benign
rs118693077019:56,002,243G/Auncertain significance
rs95183726019:56,002,300G/Auncertain significance
rs91130543219:56,002,369G/Auncertain significance
rs54010775319:56,002,376G/Cuncertain significance
rs37607285019:56,002,402C/Tuncertain significance
rs75219032319:56,002,403G/Auncertain significance
rs37012156019:56,002,406G/Cuncertain significance
rs129486252019:56,002,421G/Tuncertain significance
rs77775122019:56,002,430C/Tuncertain significance
rs14433829219:56,004,351T/Cintron variant
rs99032009619:56,004,980G/Auncertain significance
rs143655122419:56,004,988G/Auncertain significance
rs92826586019:56,005,036C/Tuncertain significance
rs128265030319:56,005,059C/Guncertain significance
rs126298323819:56,005,078G/Auncertain significance
rs133651906919:56,005,107C/Tlikely benign
rs146011290919:56,005,129G/Cuncertain significance
rs141174618319:56,005,139T/Cuncertain significance
rs127197303319:56,005,171G/Auncertain significance
rs121552952619:56,005,211T/Guncertain significance
rs132668218919:56,005,222C/Guncertain significance
rs122894793619:56,005,225C/Auncertain significance
rs126410775419:56,005,249C/Auncertain significance
rs56137499519:56,005,252C/Tuncertain significance
rs480130819:56,005,255G/Auncertain significance
rs130607596019:56,005,986T/Guncertain significance
rs54068415519:56,005,994G/Auncertain significance
rs36833836919:56,006,013C/Tuncertain significance
rs96762221119:56,006,046C/Tuncertain significance
rs37681268519:56,006,059G/Alikely benign
rs128167871519:56,006,070C/Tlikely benign
rs98582532619:56,006,076A/Guncertain significance
rs75778082119:56,006,087A/Cuncertain significance
rs77265423919:56,006,115C/Tuncertain significance
rs92456968819:56,006,123G/Auncertain significance
rs251426348119:56,006,141C/Auncertain significance
rs129353850119:56,009,262G/Cuncertain significance
rs75647914519:56,009,319G/Auncertain significance
rs198736875619:56,009,330G/Auncertain significance
rs18493073119:56,009,348G/Auncertain significance
rs89012756419:56,009,408G/Auncertain significance
rs6174894319:56,009,424G/Alikely benign
rs117591063719:56,009,483G/Cuncertain significance
rs120686648719:56,009,531G/Auncertain significance
rs75834872119:56,009,547T/Cuncertain significance
rs11152748119:56,011,203A/Guncertain significance
rs78040315819:56,011,210A/Tuncertain significance
rs96762632119:56,011,212C/Tuncertain significance
rs102829089619:56,011,231T/Cuncertain significance
rs15067064119:56,011,267C/Tuncertain significance
rs3565140619:56,011,279C/Tlikely benign
rs75254086719:56,011,291C/Tuncertain significance
rs97130211919:56,011,330C/Tuncertain significance
rs129831264919:56,011,357G/Tuncertain significance
rs37248578319:56,011,396C/Auncertain significance
rs198744092919:56,011,510C/Auncertain significance
rs127469995419:56,011,529G/Alikely benign
rs94574330619:56,011,599C/Tuncertain significance
rs54155231719:56,011,608A/Cuncertain significance
rs76079024919:56,011,630C/Tuncertain significance

Showing 100 of 180 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.