HAUS8
HAUS augmin like complex subunit 8
Summary
HAUS8 is 1 of 8 subunits of the 390-kD human augmin complex, or HAUS complex. The augmin complex was first identified in Drosophila, and its name comes from the Latin verb 'augmentare,' meaning 'to increase.' The augmin complex is a microtubule-binding complex involved in microtubule generation within the mitotic spindle and is vital to mitotic spindle assembly (Goshima et al., 2008 [PubMed 18443220]; Uehara et al., 2009 [PubMed 19369198]).[supplied by OMIM, Jun 2010]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1012299233 | 19:17,160,705 | C/T | — | likely benign |
| rs367836157 | 19:17,160,750 | T/C | — | uncertain significance |
| rs377195007 | 19:17,160,792 | G/A | — | uncertain significance |
| rs201212472 | 19:17,160,808 | C/T | — | uncertain significance |
| rs57533879 | 19:17,160,894 | G/A | — | benign |
| rs781130436 | 19:17,160,957 | G/A | — | uncertain significance |
| rs1451478667 | 19:17,163,683 | A/G | — | uncertain significance |
| rs186648625 | 19:17,163,696 | C/T | — | uncertain significance |
| rs2512643244 | 19:17,163,707 | T/C | — | uncertain significance |
| rs770170340 | 19:17,163,744 | G/A | — | uncertain significance |
| rs771781763 | 19:17,163,756 | C/A | — | uncertain significance |
| rs756896226 | 19:17,166,677 | G/C | — | uncertain significance |
| rs142481772 | 19:17,166,713 | C/T | — | uncertain significance |
| rs199724341 | 19:17,166,733 | G/A | — | uncertain significance |
| rs200201378 | 19:17,166,745 | G/A | — | uncertain significance |
| rs145956569 | 19:17,166,752 | A/T | — | uncertain significance |
| rs368580615 | 19:17,166,791 | C/T | — | uncertain significance |
| rs945735841 | 19:17,166,797 | G/A | — | uncertain significance |
| rs149256597 | 19:17,166,809 | C/T | — | uncertain significance |
| rs73504817 | 19:17,167,723 | T/G | — | — |
| rs2057339821 | 19:17,169,385 | C/T | — | uncertain significance |
| rs145244331 | 19:17,169,415 | G/A | — | uncertain significance |
| rs373422654 | 19:17,169,424 | C/T | — | uncertain significance |
| rs768842830 | 19:17,169,427 | G/A | — | uncertain significance |
| rs145277823 | 19:17,169,637 | G/A | — | uncertain significance |
| rs2512650464 | 19:17,169,650 | T/A | — | uncertain significance |
| rs147620520 | 19:17,169,660 | C/T | — | uncertain significance |
| rs572498476 | 19:17,169,673 | G/A | — | uncertain significance |
| rs201253866 | 19:17,170,440 | G/A | — | uncertain significance |
| rs73504824 | 19:17,170,451 | G/A | — | benign |
| rs777749816 | 19:17,170,896 | C/G | — | uncertain significance |
| rs1006756095 | 19:17,173,517 | T/C | — | uncertain significance |
| rs369498433 | 19:17,173,561 | C/T | — | uncertain significance |
| rs901649472 | 19:17,179,863 | T/C | — | uncertain significance |
| rs201894284 | 19:17,179,876 | G/A | — | uncertain significance |
| rs12461874 | 19:17,180,358 | C/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.