MYRIP
myosin VIIA and Rab interacting protein
Summary
Predicted to enable actin binding activity; myosin binding activity; and protein kinase A binding activity. Predicted to be involved in positive regulation of insulin secretion. Predicted to be located in several cellular components, including cytoplasmic vesicle; perinuclear region of cytoplasm; and photoreceptor outer segment. Predicted to be part of exocyst. Predicted to be active in cortical actin cytoskeleton. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants69 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs186391945 | 3:39,856,596 | T/C | intron variant | — |
| rs564525845 | 3:39,867,267 | T/C | — | — |
| rs1375669989 | 3:39,942,376 | A/T | — | uncertain significance |
| rs761963096 | 3:39,942,393 | G/A | — | uncertain significance |
| rs1599903 | 3:39,955,066 | A/T | — | — |
| rs545295648 | 3:39,997,371 | A/G | — | — |
| rs9985399 | 3:40,008,634 | T/C | upstream gene variant | — |
| rs576878406 | 3:40,052,719 | T/C | — | — |
| rs958854657 | 3:40,085,570 | G/C | — | uncertain significance |
| rs144297756 | 3:40,085,614 | C/A | — | uncertain significance |
| rs139785854 | 3:40,085,644 | A/G | — | uncertain significance |
| rs570449904 | 3:40,085,665 | C/T | — | uncertain significance |
| rs199768420 | 3:40,085,722 | C/T | — | uncertain significance |
| rs572572991 | 3:40,085,746 | G/A | — | uncertain significance |
| rs564654381 | 3:40,085,759 | C/T | — | uncertain significance |
| rs56248790 | 3:40,085,760 | G/A | — | benign |
| rs6599077 | 3:40,096,618 | G/C | — | — |
| rs188369818 | 3:40,163,178 | G/T | intron variant | — |
| rs2470879646 | 3:40,192,574 | A/G | — | uncertain significance |
| rs199884040 | 3:40,192,588 | C/T | — | uncertain significance |
| rs138774955 | 3:40,192,598 | G/T | — | uncertain significance |
| rs759162507 | 3:40,192,615 | G/A | — | uncertain significance |
| rs2470879853 | 3:40,192,628 | T/G | — | uncertain significance |
| rs142760932 | 3:40,192,666 | G/C | — | uncertain significance |
| rs763591576 | 3:40,208,337 | G/A | — | uncertain significance |
| rs763430506 | 3:40,208,417 | G/A | — | uncertain significance |
| rs141961787 | 3:40,208,683 | C/A | — | uncertain significance |
| rs144535737 | 3:40,208,734 | G/A | — | benign |
| rs747405501 | 3:40,211,544 | C/T | — | uncertain significance |
| rs376404162 | 3:40,211,573 | G/A | — | likely benign |
| rs2470949174 | 3:40,223,757 | C/G | — | uncertain significance |
| rs746841406 | 3:40,223,801 | C/G | — | uncertain significance |
| rs140013771 | 3:40,223,806 | C/A | — | likely benign |
| rs144807590 | 3:40,223,808 | C/T | — | likely benign |
| rs1160458604 | 3:40,231,412 | G/A | — | uncertain significance |
| rs199926745 | 3:40,231,416 | C/T | — | uncertain significance |
| rs71331109 | 3:40,231,417 | G/A | — | benign |
| rs149582405 | 3:40,231,451 | T/A | — | uncertain significance |
| rs374697001 | 3:40,231,475 | G/A | — | uncertain significance |
| rs759076228 | 3:40,231,523 | C/A | — | uncertain significance |
| rs201578923 | 3:40,231,593 | C/G | — | uncertain significance |
| rs138572237 | 3:40,231,688 | G/A | — | uncertain significance |
| rs1401181514 | 3:40,231,752 | T/C | — | uncertain significance |
| rs199718064 | 3:40,231,754 | C/T | — | uncertain significance |
| rs1951166887 | 3:40,231,809 | C/A | — | uncertain significance |
| rs1010215407 | 3:40,231,812 | C/T | — | uncertain significance |
| rs141497737 | 3:40,231,814 | G/A | — | uncertain significance |
| rs145932242 | 3:40,231,856 | C/T | — | uncertain significance |
| rs755428435 | 3:40,231,881 | G/A | — | uncertain significance |
| rs532025468 | 3:40,231,902 | G/A | — | uncertain significance |
| rs375455251 | 3:40,231,924 | C/A | — | uncertain significance |
| rs201954262 | 3:40,251,349 | C/T | — | uncertain significance |
| rs368575093 | 3:40,251,376 | G/A | — | uncertain significance |
| rs146905729 | 3:40,251,388 | G/A | — | likely benign |
| rs142450900 | 3:40,251,483 | G/A | — | uncertain significance |
| rs377647150 | 3:40,251,550 | A/G | — | uncertain significance |
| rs1952738224 | 3:40,275,353 | T/C | — | uncertain significance |
| rs545211502 | 3:40,275,446 | G/A | — | uncertain significance |
| rs201322608 | 3:40,275,492 | G/A | — | uncertain significance |
| rs780960761 | 3:40,286,064 | C/T | — | uncertain significance |
| rs150468012 | 3:40,286,065 | G/A | — | likely benign |
| rs749108505 | 3:40,291,732 | G/A | — | uncertain significance |
| rs774487741 | 3:40,291,750 | T/C | — | uncertain significance |
| rs192146282 | 3:40,291,779 | C/T | — | uncertain significance |
| rs750232179 | 3:40,293,389 | T/A | — | uncertain significance |
| rs200695832 | 3:40,293,402 | C/T | — | uncertain significance |
| rs2471106333 | 3:40,293,408 | A/C | — | uncertain significance |
| rs144433719 | 3:40,293,431 | C/T | — | uncertain significance |
| rs746039116 | 3:40,299,653 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.