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
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3757354 | 6:16,127,407 | C/T | regulatory region variant | — |
| rs760632 | 6:16,129,072 | A/G | regulatory region variant | — |
| rs201021082 | 6:16,129,603 | T/C | — | uncertain significance |
| rs139533286 | 6:16,129,609 | C/A | — | uncertain significance |
| rs752327773 | 6:16,129,642 | T/C | — | uncertain significance |
| rs909562 | 6:16,130,333 | A/G | regulatory region variant | — |
| rs149696224 | 6:16,130,851 | G/A | — | likely benign |
| rs1376521044 | 6:16,130,896 | A/T | — | uncertain significance |
| rs2235215 | 6:16,131,156 | T/C | regulatory region variant | — |
| rs2066905 | 6:16,131,297 | G/A | — | — |
| rs752715251 | 6:16,141,885 | C/A | — | uncertain significance |
| rs139469255 | 6:16,141,919 | G/A | — | likely benign |
| rs145292846 | 6:16,141,938 | G/T | — | uncertain significance |
| rs565497429 | 6:16,141,953 | A/T | — | uncertain significance |
| rs772572152 | 6:16,141,957 | A/T | — | uncertain significance |
| rs2532234127 | 6:16,141,961 | T/G | — | uncertain significance |
| rs753951366 | 6:16,142,050 | G/A | — | likely benign |
| rs374523605 | 6:16,143,248 | C/T | — | uncertain significance |
| rs368767683 | 6:16,143,252 | A/G | — | uncertain significance |
| rs370693513 | 6:16,143,326 | G/A | — | likely benign |
| rs2532238551 | 6:16,143,328 | C/T | — | uncertain significance |
| rs201162030 | 6:16,143,337 | A/T | — | uncertain significance |
| rs1355723926 | 6:16,143,349 | A/G | — | uncertain significance |
| rs759630605 | 6:16,143,360 | G/A | — | uncertain significance |
| rs201953912 | 6:16,143,363 | C/T | — | uncertain significance |
| rs79992066 | 6:16,143,390 | C/A | — | benign |
| rs151199797 | 6:16,143,437 | C/G | — | likely benign |
| rs2072783 | 6:16,143,897 | A/G | downstream gene variant | — |
| rs761323849 | 6:16,143,952 | A/G | — | uncertain significance |
| rs150429938 | 6:16,143,953 | T/C | — | uncertain significance |
| rs2532241842 | 6:16,143,961 | C/A | — | uncertain significance |
| rs138175799 | 6:16,143,986 | C/T | — | uncertain significance |
| rs112531050 | 6:16,143,987 | G/A | — | likely benign |
| rs112824443 | 6:16,143,988 | G/A | — | uncertain significance |
| rs770715660 | 6:16,144,053 | C/T | — | likely benign |
| rs34627146 | 6:16,144,080 | G/A | — | benign |
| rs1759730961 | 6:16,144,105 | C/A | — | likely benign |
| rs200099792 | 6:16,145,108 | T/A | — | likely benign |
| rs752855647 | 6:16,145,168 | C/T | — | uncertain significance |
| rs139029844 | 6:16,145,218 | C/A | — | uncertain significance |
| rs2532248496 | 6:16,145,284 | G/T | — | uncertain significance |
| rs1370592364 | 6:16,145,294 | A/G | — | uncertain significance |
| rs201087709 | 6:16,145,303 | G/A | — | uncertain significance |
| rs184891518 | 6:16,145,314 | C/T | — | likely benign |
| rs142124143 | 6:16,145,315 | G/A | — | likely benign |
| rs9370867 | 6:16,145,325 | A/G | missense variant | benign |
| rs2532248988 | 6:16,145,333 | A/G | — | uncertain significance |
| rs770000086 | 6:16,145,346 | C/T | — | uncertain significance |
| rs2113566382 | 6:16,145,360 | T/C | — | uncertain significance |
| rs749830853 | 6:16,145,372 | A/G | — | uncertain significance |
| rs769142887 | 6:16,145,383 | C/T | — | likely benign |
| rs148561418 | 6:16,145,389 | C/T | — | likely benign |
| rs377351131 | 6:16,145,390 | G/A | — | uncertain significance |
| rs370365355 | 6:16,145,395 | C/T | — | likely benign |
| rs141183183 | 6:16,145,414 | C/T | — | uncertain significance |
| rs113021568 | 6:16,145,419 | G/A | — | benign |
| rs374712005 | 6:16,145,431 | G/A | — | likely benign |
| rs147637310 | 6:16,145,437 | C/G | — | likely benign |
| rs1060901 | 6:16,145,473 | C/T | — | likely benign |
| rs770371971 | 6:16,145,474 | G/A | — | uncertain significance |
| rs1458670902 | 6:16,145,525 | G/A | — | uncertain significance |
| rs148878853 | 6:16,145,533 | C/T | — | likely benign |
| rs779407179 | 6:16,145,534 | G/A | — | uncertain significance |
| rs143704444 | 6:16,145,536 | C/T | — | likely benign |
| rs531259441 | 6:16,145,537 | G/A | — | likely benign |
| rs1245200112 | 6:16,145,552 | G/C | — | uncertain significance |
| rs773835321 | 6:16,145,564 | G/A | — | likely benign |
| rs1006878821 | 6:16,146,874 | G/T | — | likely benign |
| rs146590862 | 6:16,146,902 | G/A | — | uncertain significance |
| rs558704162 | 6:16,146,912 | C/T | — | uncertain significance |
| rs201093222 | 6:16,146,913 | G/A | — | likely benign |
| rs753046284 | 6:16,146,914 | C/T | — | uncertain significance |
| rs199758517 | 6:16,146,915 | G/T | — | uncertain significance |
| rs141194819 | 6:16,146,917 | G/A | — | uncertain significance |
| rs778903550 | 6:16,146,934 | C/T | — | likely benign |
| rs138820906 | 6:16,146,949 | G/A | — | likely benign |
| rs770977798 | 6:16,146,977 | A/G | — | uncertain significance |
| rs6924995 | 6:16,161,425 | A/G | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.