PSG5

pregnancy specific beta-1-glycoprotein 5

Summary

The human pregnancy-specific glycoproteins (PSGs) are a group of molecules that are mainly produced by the placental syncytiotrophoblasts during pregnancy. PSGs comprise a subgroup of the carcinoembryonic antigen (CEA) family, which belongs to the immunoglobulin superfamily. For additional general information about the PSG gene family, see PSG1 (MIM 176390).[supplied by OMIM, Oct 2009]

Known Variants40 total

rsidPosition (GRCh37)AllelesClassClinVar
rs76249693819:43,674,272C/Tlikely benign
rs36778325819:43,674,287G/Auncertain significance
rs235543319:43,679,088A/T
rs105846719:43,679,410A/Glikely benign
rs77627408019:43,679,414G/Auncertain significance
rs15058744119:43,679,421G/Auncertain significance
rs13964392919:43,679,430A/Guncertain significance
rs53292382519:43,679,449C/Auncertain significance
rs14759943119:43,679,505T/Auncertain significance
rs77491289019:43,679,534T/Cuncertain significance
rs74637077819:43,679,537G/Cuncertain significance
rs20042449319:43,680,072C/Tuncertain significance
rs74807120719:43,680,114C/Tuncertain significance
rs14043727419:43,680,144G/Auncertain significance
rs53636268219:43,680,168G/Auncertain significance
rs75907870119:43,680,195A/Guncertain significance
rs251349585919:43,680,196T/Cuncertain significance
rs76452769919:43,680,206G/Cuncertain significance
rs19950505419:43,680,215C/Tlikely benign
rs20053755319:43,680,221T/Guncertain significance
rs14246195019:43,680,235C/Guncertain significance
rs75247677719:43,680,238A/Clikely benign
rs1042008919:43,687,770C/Tintron variant
rs14360144819:43,688,960G/Auncertain significance
rs74596685119:43,688,984C/Tuncertain significance
rs251351215819:43,689,047G/Tuncertain significance
rs77084079619:43,689,051C/Tuncertain significance
rs120156903619:43,689,065G/Cuncertain significance
rs53450129519:43,689,125G/Auncertain significance
rs251351255819:43,689,142G/Tuncertain significance
rs77625276119:43,689,144C/Tuncertain significance
rs74770642719:43,689,146A/Guncertain significance
rs76115531119:43,689,261G/Cuncertain significance
rs76208581119:43,689,269A/Glikely benign
rs20191834019:43,689,303G/Alikely benign
rs52974606919:43,690,517G/Tuncertain significance
rs37250013119:43,690,523T/Cuncertain significance
rs14233846619:43,690,527G/Cuncertain significance
rs11178036619:43,690,551G/Tuncertain significance
rs11382798019:43,692,074T/A

Gene information from NCBI Gene. Variant classifications from ClinVar.