BYSL

bystin like

Summary

Bystin is expressed as a 2-kb major transcript and a 3.6-kb minor transcript in SNG-M cells and in human trophoblastic teratocarcinoma HT-H cells. Protein binding assays determined that bystin binds directly to trophinin and tastin, and that binding is enhanced when cytokeratins 8 and 18 are present. Immunocytochemistry of HT-H cells showed that bystin colocalizes with trophinin, tastin, and the cytokeratins, suggesting that these molecules form a complex in trophectoderm cells at the time of implantation. Using immunohistochemistry it was determined that trophinin and bystin are found in the placenta from the sixth week of pregnancy. Both proteins were localized in the cytoplasm of the syncytiotrophoblast in the chorionic villi and in endometrial decidual cells at the uteroplacental interface. After week 10, the levels of trophinin, tastin, and bystin decreased and then disappeared from placental villi. [provided by RefSeq, Jul 2008]

Known Variants26 total

rsidPosition (GRCh37)AllelesClassClinVar
rs1435517646:41,889,323G/Auncertain significance
rs11614081816:41,889,364C/Guncertain significance
rs5632535096:41,889,487C/Tuncertain significance
rs17754836526:41,889,560C/Tuncertain significance
rs24797246:41,890,982T/Cupstream gene variant
rs25331298806:41,895,117A/Glikely benign
rs361241886:41,895,193C/Tbenign
rs7657818216:41,897,872G/Auncertain significance
rs7509107306:41,897,922G/Auncertain significance
rs25331347766:41,897,927G/Cuncertain significance
rs7812570706:41,898,004G/Auncertain significance
rs7543539456:41,898,379T/Cuncertain significance
rs5527303666:41,898,388C/Tuncertain significance
rs3758675926:41,898,389G/Tuncertain significance
rs7513783386:41,898,430C/Tuncertain significance
rs7570620816:41,898,437A/Guncertain significance
rs1433819286:41,899,213G/Alikely benign
rs3682341376:41,899,229G/Auncertain significance
rs7500266986:41,899,519A/Guncertain significance
rs25331391296:41,900,142A/Tuncertain significance
rs1498710946:41,900,347G/Auncertain significance
rs1495875486:41,900,375C/Glikely benign
rs1406323196:41,900,410G/Auncertain significance
rs5513745116:41,900,415G/Auncertain significance
rs13026085946:41,900,421G/Auncertain significance
rs10531336:41,900,625C/T

Gene information from NCBI Gene. Variant classifications from ClinVar.