MYLIP

myosin regulatory light chain interacting protein

Summary

The ERM protein family members ezrin, radixin, and moesin are cytoskeletal effector proteins linking actin to membrane-bound proteins at the cell surface. Myosin regulatory light chain interacting protein (MYLIP) is a novel ERM-like protein that interacts with myosin regulatory light chain and inhibits neurite outgrowth. [provided by RefSeq, Jul 2008]

Known Variants78 total

rsidPosition (GRCh37)AllelesClassClinVar
rs37573546:16,127,407C/Tregulatory region variant—
rs7606326:16,129,072A/Gregulatory region variant—
rs2010210826:16,129,603T/C—uncertain significance
rs1395332866:16,129,609C/A—uncertain significance
rs7523277736:16,129,642T/C—uncertain significance
rs9095626:16,130,333A/Gregulatory region variant—
rs1496962246:16,130,851G/A—likely benign
rs13765210446:16,130,896A/T—uncertain significance
rs22352156:16,131,156T/Cregulatory region variant—
rs20669056:16,131,297G/A——
rs7527152516:16,141,885C/A—uncertain significance
rs1394692556:16,141,919G/A—likely benign
rs1452928466:16,141,938G/T—uncertain significance
rs5654974296:16,141,953A/T—uncertain significance
rs7725721526:16,141,957A/T—uncertain significance
rs25322341276:16,141,961T/G—uncertain significance
rs7539513666:16,142,050G/A—likely benign
rs3745236056:16,143,248C/T—uncertain significance
rs3687676836:16,143,252A/G—uncertain significance
rs3706935136:16,143,326G/A—likely benign
rs25322385516:16,143,328C/T—uncertain significance
rs2011620306:16,143,337A/T—uncertain significance
rs13557239266:16,143,349A/G—uncertain significance
rs7596306056:16,143,360G/A—uncertain significance
rs2019539126:16,143,363C/T—uncertain significance
rs799920666:16,143,390C/A—benign
rs1511997976:16,143,437C/G—likely benign
rs20727836:16,143,897A/Gdownstream gene variant—
rs7613238496:16,143,952A/G—uncertain significance
rs1504299386:16,143,953T/C—uncertain significance
rs25322418426:16,143,961C/A—uncertain significance
rs1381757996:16,143,986C/T—uncertain significance
rs1125310506:16,143,987G/A—likely benign
rs1128244436:16,143,988G/A—uncertain significance
rs7707156606:16,144,053C/T—likely benign
rs346271466:16,144,080G/A—benign
rs17597309616:16,144,105C/A—likely benign
rs2000997926:16,145,108T/A—likely benign
rs7528556476:16,145,168C/T—uncertain significance
rs1390298446:16,145,218C/A—uncertain significance
rs25322484966:16,145,284G/T—uncertain significance
rs13705923646:16,145,294A/G—uncertain significance
rs2010877096:16,145,303G/A—uncertain significance
rs1848915186:16,145,314C/T—likely benign
rs1421241436:16,145,315G/A—likely benign
rs93708676:16,145,325A/Gmissense variantbenign
rs25322489886:16,145,333A/G—uncertain significance
rs7700000866:16,145,346C/T—uncertain significance
rs21135663826:16,145,360T/C—uncertain significance
rs7498308536:16,145,372A/G—uncertain significance
rs7691428876:16,145,383C/T—likely benign
rs1485614186:16,145,389C/T—likely benign
rs3773511316:16,145,390G/A—uncertain significance
rs3703653556:16,145,395C/T—likely benign
rs1411831836:16,145,414C/T—uncertain significance
rs1130215686:16,145,419G/A—benign
rs3747120056:16,145,431G/A—likely benign
rs1476373106:16,145,437C/G—likely benign
rs10609016:16,145,473C/T—likely benign
rs7703719716:16,145,474G/A—uncertain significance
rs14586709026:16,145,525G/A—uncertain significance
rs1488788536:16,145,533C/T—likely benign
rs7794071796:16,145,534G/A—uncertain significance
rs1437044446:16,145,536C/T—likely benign
rs5312594416:16,145,537G/A—likely benign
rs12452001126:16,145,552G/C—uncertain significance
rs7738353216:16,145,564G/A—likely benign
rs10068788216:16,146,874G/T—likely benign
rs1465908626:16,146,902G/A—uncertain significance
rs5587041626:16,146,912C/T—uncertain significance
rs2010932226:16,146,913G/A—likely benign
rs7530462846:16,146,914C/T—uncertain significance
rs1997585176:16,146,915G/T—uncertain significance
rs1411948196:16,146,917G/A—uncertain significance
rs7789035506:16,146,934C/T—likely benign
rs1388209066:16,146,949G/A—likely benign
rs7709777986:16,146,977A/G—uncertain significance
rs69249956:16,161,425A/Gcoding sequence variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.

MYLIP — myosin regulatory light chain interacting protein