TOGARAM2
TOG array regulator of axonemal microtubules 2
Summary
Predicted to enable microtubule binding activity. Predicted to be involved in microtubule cytoskeleton organization. Predicted to be located in microtubule cytoskeleton. Predicted to be active in cilium and cytoplasmic microtubule. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants93 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs144788540 | 2:29,190,221 | G/A | intron variant | — |
| rs370559743 | 2:29,221,053 | C/T | — | uncertain significance |
| rs1466627295 | 2:29,221,107 | C/T | — | uncertain significance |
| rs535501769 | 2:29,222,085 | G/A | — | uncertain significance |
| rs760125956 | 2:29,222,091 | C/T | — | uncertain significance |
| rs2465555907 | 2:29,222,110 | G/T | — | uncertain significance |
| rs573115970 | 2:29,222,116 | G/A | — | uncertain significance |
| rs771852665 | 2:29,222,139 | G/C | — | uncertain significance |
| rs756709437 | 2:29,222,230 | C/T | — | uncertain significance |
| rs746770883 | 2:29,222,256 | G/C | — | uncertain significance |
| rs376738396 | 2:29,222,299 | G/A | — | uncertain significance |
| rs373609639 | 2:29,225,443 | C/T | — | uncertain significance |
| rs202118942 | 2:29,225,589 | C/G | — | likely benign |
| rs757999432 | 2:29,226,359 | C/T | — | likely benign |
| rs749653932 | 2:29,226,383 | A/G | — | uncertain significance |
| rs543434094 | 2:29,226,418 | G/A | — | uncertain significance |
| rs766401480 | 2:29,226,452 | C/T | — | uncertain significance |
| rs201280601 | 2:29,226,473 | G/A | — | uncertain significance |
| rs200094591 | 2:29,234,331 | G/A | — | uncertain significance |
| rs200807676 | 2:29,234,351 | G/T | — | uncertain significance |
| rs769133714 | 2:29,237,313 | G/T | — | uncertain significance |
| rs146532049 | 2:29,237,314 | C/A | — | uncertain significance |
| rs770702588 | 2:29,237,317 | G/A | — | uncertain significance |
| rs564518939 | 2:29,237,342 | C/T | — | uncertain significance |
| rs757275245 | 2:29,237,345 | C/T | — | uncertain significance |
| rs751392022 | 2:29,237,357 | T/C | — | uncertain significance |
| rs781127093 | 2:29,237,371 | G/A | — | uncertain significance |
| rs144989786 | 2:29,237,425 | A/G | — | uncertain significance |
| rs1351684464 | 2:29,240,029 | A/G | — | uncertain significance |
| rs763440132 | 2:29,240,040 | G/C | — | uncertain significance |
| rs543539008 | 2:29,240,047 | C/T | — | uncertain significance |
| rs1664632671 | 2:29,240,069 | A/C | — | uncertain significance |
| rs201395358 | 2:29,240,085 | G/C | — | uncertain significance |
| rs752298206 | 2:29,240,721 | G/A | — | uncertain significance |
| rs1358271372 | 2:29,240,758 | C/G | — | uncertain significance |
| rs376977904 | 2:29,240,759 | C/T | — | uncertain significance |
| rs770863060 | 2:29,240,762 | G/A | — | likely benign |
| rs373667686 | 2:29,240,777 | A/T | — | uncertain significance |
| rs201222928 | 2:29,240,784 | T/C | — | uncertain significance |
| rs376986385 | 2:29,240,802 | G/A | — | uncertain significance |
| rs745859696 | 2:29,240,810 | C/T | — | uncertain significance |
| rs202165946 | 2:29,245,036 | C/T | — | uncertain significance |
| rs2465728696 | 2:29,245,089 | C/T | — | uncertain significance |
| rs772507909 | 2:29,245,120 | C/T | — | uncertain significance |
| rs929758807 | 2:29,245,983 | C/T | — | conflicting classifications of pathogenicity |
| rs765920057 | 2:29,247,086 | G/A | — | uncertain significance |
| rs370731705 | 2:29,247,095 | G/T | — | uncertain significance |
| rs189990269 | 2:29,247,143 | G/A | — | uncertain significance |
| rs200564513 | 2:29,247,177 | G/A | — | uncertain significance |
| rs201981896 | 2:29,247,206 | C/T | — | uncertain significance |
| rs999139067 | 2:29,247,221 | C/T | — | uncertain significance |
| rs13008299 | 2:29,247,997 | T/G | intron variant | — |
| rs755063375 | 2:29,249,738 | C/T | — | uncertain significance |
| rs189858078 | 2:29,249,755 | G/A | — | likely benign |
| rs1254209226 | 2:29,249,756 | C/T | — | uncertain significance |
| rs771502029 | 2:29,249,768 | G/A | — | uncertain significance |
| rs774945093 | 2:29,249,798 | C/A | — | uncertain significance |
| rs2465788464 | 2:29,255,801 | T/C | — | uncertain significance |
| rs531335768 | 2:29,255,810 | C/T | — | uncertain significance |
| rs1180267885 | 2:29,255,830 | G/C | — | uncertain significance |
| rs185690145 | 2:29,256,347 | A/G | — | uncertain significance |
| rs2465791843 | 2:29,256,359 | C/T | — | uncertain significance |
| rs762657492 | 2:29,256,375 | G/A | — | likely benign |
| rs2465800584 | 2:29,258,346 | C/T | — | uncertain significance |
| rs139312547 | 2:29,258,364 | C/T | — | uncertain significance |
| rs200703318 | 2:29,258,365 | G/A | — | uncertain significance |
| rs149588231 | 2:29,258,394 | G/A | — | uncertain significance |
| rs202000034 | 2:29,258,419 | G/A | — | uncertain significance |
| rs201166546 | 2:29,258,434 | A/G | — | uncertain significance |
| rs1250595351 | 2:29,258,502 | G/C | — | uncertain significance |
| rs577316734 | 2:29,258,505 | A/G | — | likely benign |
| rs368441564 | 2:29,259,465 | C/T | — | uncertain significance |
| rs183105380 | 2:29,259,530 | A/G | — | uncertain significance |
| rs770935644 | 2:29,259,584 | G/A | — | uncertain significance |
| rs760807481 | 2:29,259,590 | G/A | — | uncertain significance |
| rs147929389 | 2:29,259,594 | C/T | — | uncertain significance |
| rs150485801 | 2:29,259,606 | C/T | — | likely benign |
| rs756772607 | 2:29,268,228 | C/T | — | uncertain significance |
| rs746449071 | 2:29,268,233 | C/A | — | uncertain significance |
| rs150801790 | 2:29,268,244 | G/A | — | uncertain significance |
| rs562680249 | 2:29,268,250 | T/G | — | uncertain significance |
| rs149465089 | 2:29,268,267 | C/T | — | uncertain significance |
| rs544155983 | 2:29,274,663 | G/C | — | uncertain significance |
| rs766775148 | 2:29,274,666 | C/T | — | uncertain significance |
| rs752786793 | 2:29,274,705 | G/A | — | likely benign |
| rs200360935 | 2:29,274,729 | G/A | — | uncertain significance |
| rs2465856150 | 2:29,274,732 | C/A | — | uncertain significance |
| rs376723895 | 2:29,274,748 | G/T | — | uncertain significance |
| rs757455935 | 2:29,274,763 | G/A | — | uncertain significance |
| rs200413260 | 2:29,274,799 | G/A | — | uncertain significance |
| rs769447595 | 2:29,274,816 | G/A | — | uncertain significance |
| rs566868772 | 2:29,274,871 | C/T | — | uncertain significance |
| rs2465857097 | 2:29,274,934 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.