INCENP
inner centromere protein
Summary
In mammalian cells, 2 broad groups of centromere-interacting proteins have been described: constitutively binding centromere proteins and 'passenger,' or transiently interacting, proteins (reviewed by Choo, 1997). The constitutive proteins include CENPA (centromere protein A; MIM 117139), CENPB (MIM 117140), CENPC1 (MIM 117141), and CENPD (MIM 117142). The term 'passenger proteins' encompasses a broad collection of proteins that localize to the centromere during specific stages of the cell cycle (Earnshaw and Mackay, 1994 [PubMed 8088460]). These include CENPE (MIM 117143); MCAK (MIM 604538); KID (MIM 603213); cytoplasmic dynein (e.g., MIM 600112); CliPs (e.g., MIM 179838); and CENPF/mitosin (MIM 600236). The inner centromere proteins (INCENPs) (Earnshaw and Cooke, 1991 [PubMed 1860899]), the initial members of the passenger protein group, display a broad localization along chromosomes in the early stages of mitosis but gradually become concentrated at centromeres as the cell cycle progresses into mid-metaphase. During telophase, the proteins are located within the midbody in the intercellular bridge, where they are discarded after cytokinesis (Cutts et al., 1999 [PubMed 10369859]).[supplied by OMIM, Mar 2008]
Known Variants170 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs79215615 | 11:61,895,444 | A/G | — | — |
| rs3825035 | 11:61,895,476 | A/G | — | benign |
| rs1675130 | 11:61,895,541 | G/A | — | benign |
| rs779937744 | 11:61,895,644 | C/T | — | uncertain significance |
| rs927507409 | 11:61,895,649 | C/T | — | uncertain significance |
| rs1457978482 | 11:61,895,670 | G/A | — | uncertain significance |
| rs917711276 | 11:61,895,718 | A/G | — | uncertain significance |
| rs1675131 | 11:61,895,741 | G/A | — | benign |
| rs1260396107 | 11:61,895,754 | G/T | — | uncertain significance |
| rs748187082 | 11:61,895,761 | G/A | — | uncertain significance |
| rs1792946 | 11:61,896,215 | G/A | — | benign |
| rs1943813988 | 11:61,896,259 | C/T | — | uncertain significance |
| rs1943814490 | 11:61,896,277 | C/T | — | uncertain significance |
| rs772539906 | 11:61,896,295 | G/A | — | uncertain significance |
| rs1675132 | 11:61,896,589 | T/G | — | benign |
| rs61893661 | 11:61,897,073 | T/C | — | benign |
| rs1792944 | 11:61,897,197 | C/T | — | benign |
| rs769445442 | 11:61,897,254 | G/T | — | uncertain significance |
| rs139054193 | 11:61,897,273 | C/T | — | uncertain significance |
| rs369742634 | 11:61,897,274 | G/A | — | uncertain significance |
| rs373398703 | 11:61,897,286 | T/C | — | uncertain significance |
| rs200416661 | 11:61,897,292 | C/T | — | uncertain significance |
| rs146465225 | 11:61,897,295 | G/A | — | uncertain significance |
| rs12281503 | 11:61,897,298 | G/A | — | benign |
| rs1027885646 | 11:61,897,326 | G/T | — | uncertain significance |
| rs1675133 | 11:61,897,359 | T/C | — | benign |
| rs772094693 | 11:61,897,376 | G/A | — | uncertain significance |
| rs773254306 | 11:61,897,382 | C/T | — | uncertain significance |
| rs147033848 | 11:61,897,396 | G/A | — | uncertain significance |
| rs112218336 | 11:61,897,404 | T/C | — | benign |
| rs34441559 | 11:61,897,409 | C/T | — | benign |
| rs2541532237 | 11:61,897,415 | C/T | — | uncertain significance |
| rs34210125 | 11:61,897,468 | G/A | — | benign |
| rs533613179 | 11:61,897,495 | G/T | — | uncertain significance |
| rs777641583 | 11:61,897,526 | G/A | — | uncertain significance |
| rs202093810 | 11:61,897,567 | G/A | — | uncertain significance |
| rs143235997 | 11:61,897,618 | A/G | — | likely benign |
| rs763857838 | 11:61,897,621 | T/C | — | uncertain significance |
| rs565090054 | 11:61,897,634 | C/T | missense variant | — |
| rs762580001 | 11:61,897,715 | C/T | — | uncertain significance |
| rs139914074 | 11:61,897,739 | G/T | — | uncertain significance |
| rs149820986 | 11:61,897,753 | C/T | — | uncertain significance |
| rs2541534982 | 11:61,897,811 | C/G | — | likely benign |
| rs199734316 | 11:61,897,838 | G/A | — | uncertain significance |
| rs148320735 | 11:61,897,840 | G/T | — | uncertain significance |
| rs2541535264 | 11:61,897,873 | A/G | — | uncertain significance |
| rs1300680526 | 11:61,897,875 | G/A | — | likely benign |
| rs538914404 | 11:61,897,907 | T/G | — | uncertain significance |
| rs780332581 | 11:61,897,924 | G/A | — | uncertain significance |
| rs746543284 | 11:61,897,937 | C/T | — | likely benign |
| rs144514553 | 11:61,897,948 | G/A | — | uncertain significance |
| rs779427138 | 11:61,898,021 | A/G | — | uncertain significance |
| rs543975115 | 11:61,898,044 | G/C | — | uncertain significance |
| rs74744349 | 11:61,898,174 | C/T | — | benign |
| rs1792943 | 11:61,898,192 | G/A | — | benign |
| rs564497568 | 11:61,903,766 | A/G | — | — |
| rs116956494 | 11:61,905,129 | C/T | intron variant | — |
| rs2541553517 | 11:61,905,299 | C/G | — | uncertain significance |
| rs574706617 | 11:61,905,351 | G/T | — | uncertain significance |
| rs12271714 | 11:61,905,985 | G/A | — | benign |
| rs61751226 | 11:61,906,216 | G/A | — | benign |
| rs1184290855 | 11:61,906,223 | T/G | — | uncertain significance |
| rs1614060 | 11:61,906,299 | A/G | — | benign |
| rs1675126 | 11:61,906,374 | T/C | synonymous variant | benign |
| rs199829775 | 11:61,906,403 | C/T | — | uncertain significance |
| rs2541557714 | 11:61,906,411 | G/A | — | uncertain significance |
| rs11230922 | 11:61,906,538 | G/A | — | benign |
| rs3741246 | 11:61,907,631 | T/A | — | benign |
| rs144117865 | 11:61,907,716 | G/A | — | benign |
| rs61893679 | 11:61,907,821 | C/A | — | benign |
| rs1675124 | 11:61,907,909 | G/A | — | benign |
| rs12795611 | 11:61,907,969 | C/T | — | benign |
| rs61893680 | 11:61,908,022 | G/A | — | benign |
| rs764321537 | 11:61,908,177 | A/G | — | uncertain significance |
| rs141577121 | 11:61,908,184 | G/A | — | uncertain significance |
| rs745677768 | 11:61,908,219 | G/C | — | uncertain significance |
| rs137984629 | 11:61,908,267 | C/G | — | uncertain significance |
| rs777207002 | 11:61,908,280 | G/T | — | uncertain significance |
| rs769844773 | 11:61,908,400 | C/T | — | uncertain significance |
| rs1209187119 | 11:61,908,409 | C/G | — | uncertain significance |
| rs2277283 | 11:61,908,440 | C/T | — | benign |
| rs144797386 | 11:61,908,441 | G/A | — | uncertain significance |
| rs766161230 | 11:61,908,466 | G/A | — | uncertain significance |
| rs73499250 | 11:61,908,524 | T/G | — | benign |
| rs1675123 | 11:61,908,672 | A/G | — | benign |
| rs59139531 | 11:61,912,210 | C/T | — | benign |
| rs898382 | 11:61,912,400 | G/A | — | benign |
| rs140112279 | 11:61,912,463 | C/T | — | uncertain significance |
| rs201357288 | 11:61,912,464 | G/A | — | uncertain significance |
| rs1338854471 | 11:61,912,518 | A/T | — | uncertain significance |
| rs997363141 | 11:61,912,538 | C/T | — | uncertain significance |
| rs1944214466 | 11:61,912,657 | C/G | — | uncertain significance |
| rs768907485 | 11:61,912,673 | A/G | — | uncertain significance |
| rs1304608720 | 11:61,912,708 | A/C | — | uncertain significance |
| rs199785199 | 11:61,912,753 | A/G | — | uncertain significance |
| rs1792925 | 11:61,913,079 | C/T | — | benign |
| rs77765284 | 11:61,913,091 | G/C | — | benign |
| rs377759920 | 11:61,913,113 | C/T | — | uncertain significance |
| rs116462742 | 11:61,913,144 | C/T | — | benign |
| rs140505440 | 11:61,913,177 | G/A | — | uncertain significance |
Showing 100 of 170 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.