TTLL12
tubulin tyrosine ligase like 12
Summary
Enables histone H4K20me3 reader activity and tubulin binding activity. Involved in negative regulation of type I interferon-mediated signaling pathway and regulation of mitotic cell cycle. Located in cytosol and plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants67 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200016238 | 22:43,564,031 | C/T | — | uncertain significance |
| rs143222034 | 22:43,564,095 | G/A | — | likely benign |
| rs1252241740 | 22:43,564,154 | T/C | — | uncertain significance |
| rs367694491 | 22:43,564,789 | C/G | — | likely benign |
| rs34490661 | 22:43,564,790 | G/T | — | uncertain significance |
| rs145496614 | 22:43,564,814 | G/A | — | benign |
| rs150540626 | 22:43,564,886 | G/T | — | uncertain significance |
| rs746375120 | 22:43,564,905 | C/T | — | likely benign |
| rs371460098 | 22:43,564,912 | T/C | — | uncertain significance |
| rs117616050 | 22:43,564,923 | G/T | — | benign |
| rs201855582 | 22:43,565,524 | A/C | — | uncertain significance |
| rs1345346270 | 22:43,565,549 | T/A | — | uncertain significance |
| rs199848007 | 22:43,565,550 | C/T | — | uncertain significance |
| rs200261136 | 22:43,567,841 | T/C | — | uncertain significance |
| rs17003543 | 22:43,567,861 | C/T | — | benign |
| rs543794352 | 22:43,567,891 | G/C | — | uncertain significance |
| rs751325024 | 22:43,568,443 | C/T | — | uncertain significance |
| rs201676990 | 22:43,568,520 | C/T | — | uncertain significance |
| rs764103208 | 22:43,568,527 | A/G | — | uncertain significance |
| rs745411382 | 22:43,569,750 | T/C | — | uncertain significance |
| rs149781023 | 22:43,569,761 | C/T | — | likely benign |
| rs1363044102 | 22:43,569,768 | T/C | — | uncertain significance |
| rs776233681 | 22:43,569,771 | C/T | — | likely benign |
| rs139697412 | 22:43,569,775 | G/C | — | likely benign |
| rs199982346 | 22:43,569,789 | G/A | — | uncertain significance |
| rs140453869 | 22:43,569,790 | C/T | — | likely benign |
| rs141200040 | 22:43,570,301 | G/A | — | benign |
| rs143374565 | 22:43,570,326 | G/T | — | uncertain significance |
| rs776096968 | 22:43,570,387 | C/G | — | uncertain significance |
| rs369903948 | 22:43,570,520 | T/C | — | uncertain significance |
| rs771928793 | 22:43,570,545 | C/T | — | uncertain significance |
| rs765755267 | 22:43,570,566 | G/A | — | likely benign |
| rs1189540494 | 22:43,570,577 | G/A | — | uncertain significance |
| rs142342521 | 22:43,572,332 | A/G | — | uncertain significance |
| rs370790103 | 22:43,572,362 | A/G | — | uncertain significance |
| rs2518146215 | 22:43,572,364 | G/T | — | uncertain significance |
| rs140875180 | 22:43,572,378 | T/G | — | uncertain significance |
| rs202216754 | 22:43,572,402 | C/T | — | uncertain significance |
| rs148865013 | 22:43,575,644 | G/A | — | uncertain significance |
| rs2147074196 | 22:43,575,754 | C/T | — | likely benign |
| rs974262771 | 22:43,575,923 | G/A | — | likely benign |
| rs199520351 | 22:43,575,926 | G/T | — | uncertain significance |
| rs2518148637 | 22:43,575,933 | G/A | — | uncertain significance |
| rs148175933 | 22:43,575,954 | C/T | — | uncertain significance |
| rs774813503 | 22:43,575,955 | G/A | — | uncertain significance |
| rs142003726 | 22:43,575,956 | C/T | — | likely benign |
| rs764381591 | 22:43,576,803 | G/T | — | likely benign |
| rs199782496 | 22:43,576,816 | T/C | — | likely benign |
| rs753018642 | 22:43,576,931 | G/C | — | uncertain significance |
| rs779710957 | 22:43,578,993 | G/A | — | uncertain significance |
| rs13058467 | 22:43,579,049 | T/C | missense variant | — |
| rs150601768 | 22:43,579,055 | G/A | — | uncertain significance |
| rs145807587 | 22:43,579,073 | C/T | — | uncertain significance |
| rs765617531 | 22:43,579,077 | C/T | — | uncertain significance |
| rs59963284 | 22:43,579,081 | C/T | — | benign |
| rs767237272 | 22:43,579,082 | C/T | — | likely benign |
| rs764196779 | 22:43,579,098 | C/T | — | uncertain significance |
| rs2518151331 | 22:43,579,142 | C/G | — | uncertain significance |
| rs1932198784 | 22:43,582,904 | G/C | — | uncertain significance |
| rs775332035 | 22:43,582,981 | G/A | — | uncertain significance |
| rs1932201538 | 22:43,582,987 | T/G | — | uncertain significance |
| rs1932202049 | 22:43,582,999 | T/G | — | uncertain significance |
| rs1451722253 | 22:43,583,002 | G/A | — | uncertain significance |
| rs1247020745 | 22:43,583,048 | G/C | — | uncertain significance |
| rs529496470 | 22:43,583,062 | C/T | — | uncertain significance |
| rs1219697882 | 22:43,583,066 | C/G | — | uncertain significance |
| rs9612021 | 22:43,583,598 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.