MIP
major intrinsic protein of lens fiber
Summary
Major intrinsic protein is a member of the water-transporting aquaporins as well as the original member of the MIP family of channel proteins. The function of the fiber cell membrane protein encoded by this gene is undetermined, yet this protein is speculated to play a role in intracellular communication. The MIP protein is expressed in the ocular lens and is required for correct lens function. This gene has been mapped among aquaporins AQP2, AQP5, and AQP6, in a potential gene cluster at 12q13. [provided by RefSeq, Jul 2008]
Known Variants79 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs769951572 | 12:56,843,569 | A/G | — | uncertain significance |
| rs181959264 | 12:56,843,691 | T/C | — | benign |
| rs1868534260 | 12:56,843,802 | G/C | — | uncertain significance |
| rs2371455 | 12:56,843,893 | T/G | — | benign |
| rs72478921 | 12:56,843,960 | A/T | — | benign |
| rs886049689 | 12:56,843,961 | G/A | — | uncertain significance |
| rs543075454 | 12:56,844,095 | C/T | — | uncertain significance |
| rs924408819 | 12:56,844,107 | C/T | — | uncertain significance |
| rs1043213686 | 12:56,844,109 | C/T | — | uncertain significance |
| rs140453442 | 12:56,844,265 | T/C | — | benign |
| rs891386760 | 12:56,844,271 | G/T | — | uncertain significance |
| rs66826398 | 12:56,844,290 | C/G | — | likely benign |
| rs3809125 | 12:56,844,349 | C/T | — | benign |
| rs150155933 | 12:56,844,390 | C/T | — | uncertain significance |
| rs1470004718 | 12:56,844,403 | G/A | — | uncertain significance |
| rs17118657 | 12:56,844,449 | T/C | — | benign |
| rs565229690 | 12:56,844,463 | C/T | — | uncertain significance |
| rs1400800798 | 12:56,844,522 | G/A | — | uncertain significance |
| rs774053 | 12:56,844,559 | G/A | — | benign |
| rs137926387 | 12:56,844,573 | T/G | — | benign |
| rs72478920 | 12:56,844,657 | T/C | — | benign |
| rs886049690 | 12:56,844,722 | G/A | — | uncertain significance |
| rs148601602 | 12:56,844,780 | G/A | — | likely benign |
| rs1481521864 | 12:56,844,928 | A/C | — | uncertain significance |
| rs2935008 | 12:56,844,970 | A/C | — | benign |
| rs746044208 | 12:56,845,015 | C/T | — | likely benign |
| rs185699444 | 12:56,845,032 | A/G | — | benign |
| rs750645433 | 12:56,845,106 | C/A | — | uncertain significance |
| rs778691975 | 12:56,845,142 | C/T | — | likely benign |
| rs755752015 | 12:56,845,143 | T/G | — | uncertain significance |
| rs1555179699 | 12:56,845,158 | C/T | — | pathogenic |
| rs773085032 | 12:56,845,162 | C/G | — | uncertain significance |
| rs1349100721 | 12:56,845,218 | C/T | — | uncertain significance |
| rs1114167315 | 12:56,845,225 | C/A | — | pathogenic |
| rs2547312090 | 12:56,845,241 | C/T | — | pathogenic |
| rs2643622 | 12:56,845,296 | T/C | — | benign |
| rs2088155 | 12:56,845,303 | A/G | — | benign |
| rs7953824 | 12:56,845,358 | C/T | — | benign |
| rs112423932 | 12:56,845,401 | C/T | — | benign |
| rs113738136 | 12:56,845,478 | T/G | — | benign |
| rs1220143491 | 12:56,846,855 | C/G | — | pathogenic |
| rs2547312839 | 12:56,846,857 | C/T | — | pathogenic |
| rs766714787 | 12:56,846,878 | G/C | — | uncertain significance |
| rs759746926 | 12:56,846,902 | C/A | — | uncertain significance |
| rs1044812718 | 12:56,846,938 | T/G | — | pathogenic |
| rs56184801 | 12:56,847,061 | C/A | — | likely benign |
| rs1868687508 | 12:56,847,374 | C/T | — | likely pathogenic |
| rs36032520 | 12:56,847,384 | G/A | — | benign |
| rs1868688639 | 12:56,847,394 | G/T | — | uncertain significance |
| rs886049692 | 12:56,847,407 | C/T | — | uncertain significance |
| rs149279854 | 12:56,847,410 | C/T | — | likely benign |
| rs1868689296 | 12:56,847,412 | G/T | — | uncertain significance |
| rs779658566 | 12:56,847,442 | C/T | — | uncertain significance |
| rs1007727858 | 12:56,847,449 | C/T | — | uncertain significance |
| rs1868692984 | 12:56,847,467 | T/G | — | uncertain significance |
| rs966166555 | 12:56,847,476 | C/T | — | uncertain significance |
| rs1555179889 | 12:56,847,482 | G/T | — | uncertain significance |
| rs121917867 | 12:56,847,487 | G/C | missense variant | pathogenic |
| rs121917869 | 12:56,847,499 | T/C | missense variant | pathogenic |
| rs35033450 | 12:56,847,522 | G/A | — | likely benign |
| rs886049693 | 12:56,847,549 | G/A | — | uncertain significance |
| rs74094743 | 12:56,847,935 | G/T | — | likely benign |
| rs774928445 | 12:56,848,060 | C/T | — | uncertain significance |
| rs760722691 | 12:56,848,075 | G/A | — | uncertain significance |
| rs74641138 | 12:56,848,079 | C/T | — | likely benign |
| rs559008561 | 12:56,848,130 | T/C | — | uncertain significance |
| rs77163805 | 12:56,848,199 | C/T | — | benign |
| rs1205062502 | 12:56,848,216 | T/C | — | uncertain significance |
| rs2547313773 | 12:56,848,226 | A/C | — | uncertain significance |
| rs1436119727 | 12:56,848,279 | T/C | — | uncertain significance |
| rs139963297 | 12:56,848,300 | C/T | — | likely benign |
| rs864309693 | 12:56,848,301 | G/A | missense variant | pathogenic |
| rs757336397 | 12:56,848,364 | C/A | — | uncertain significance |
| rs201697509 | 12:56,848,378 | G/A | — | uncertain significance |
| rs1001940981 | 12:56,848,384 | C/T | — | uncertain significance |
| rs117788190 | 12:56,848,401 | A/G | — | likely benign |
| rs61759527 | 12:56,848,407 | G/T | — | likely benign |
| rs1172594016 | 12:56,848,423 | G/T | — | uncertain significance |
| rs2269348 | 12:56,848,481 | T/C | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.