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

Gene information from NCBI Gene. Variant classifications from ClinVar.