AXDND1
axonemal dynein light chain domain containing 1
Summary
Predicted to be involved in manchette assembly. Located in ciliary basal body and cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs776807443 | 1:179,335,682 | C/G | — | uncertain significance |
| rs758831558 | 1:179,335,687 | T/A | — | uncertain significance |
| rs748025457 | 1:179,337,964 | A/G | — | uncertain significance |
| rs142839599 | 1:179,338,048 | G/A | — | uncertain significance |
| rs149978532 | 1:179,338,052 | A/G | — | uncertain significance |
| rs1233475776 | 1:179,338,102 | C/T | — | uncertain significance |
| rs975025 | 1:179,338,327 | C/T | downstream gene variant | — |
| rs150327590 | 1:179,347,845 | T/G | — | uncertain significance |
| rs199947499 | 1:179,347,852 | G/A | — | likely benign |
| rs372646870 | 1:179,348,598 | G/T | — | uncertain significance |
| rs778867127 | 1:179,352,592 | A/C | — | uncertain significance |
| rs2525348114 | 1:179,352,626 | A/G | — | uncertain significance |
| rs147412323 | 1:179,352,648 | T/A | — | uncertain significance |
| rs185658017 | 1:179,352,675 | C/G | — | uncertain significance |
| rs2525380129 | 1:179,354,392 | T/C | — | uncertain significance |
| rs146917473 | 1:179,363,111 | C/T | — | likely pathogenic |
| rs752752345 | 1:179,363,145 | A/G | — | uncertain significance |
| rs747815360 | 1:179,364,250 | G/A | — | uncertain significance |
| rs147693539 | 1:179,364,256 | A/G | — | uncertain significance |
| rs182777447 | 1:179,375,268 | T/C | intron variant | — |
| rs901863349 | 1:179,380,284 | A/G | — | likely benign |
| rs751176208 | 1:179,380,288 | G/A | — | uncertain significance |
| rs371463369 | 1:179,380,297 | C/A | — | uncertain significance |
| rs569825439 | 1:179,380,306 | T/C | — | uncertain significance |
| rs2525834931 | 1:179,380,319 | G/T | — | uncertain significance |
| rs2525837854 | 1:179,380,382 | C/T | — | uncertain significance |
| rs2525838060 | 1:179,380,385 | A/G | — | uncertain significance |
| rs770158450 | 1:179,398,653 | G/A | — | uncertain significance |
| rs776126305 | 1:179,398,737 | A/G | — | uncertain significance |
| rs2526243244 | 1:179,399,681 | C/G | — | uncertain significance |
| rs1296902872 | 1:179,399,687 | G/A | — | uncertain significance |
| rs768020643 | 1:179,414,225 | C/T | — | uncertain significance |
| rs144267093 | 1:179,414,294 | C/A | — | uncertain significance |
| rs768635158 | 1:179,414,322 | G/A | — | uncertain significance |
| rs145068225 | 1:179,414,334 | A/G | — | uncertain significance |
| rs374001746 | 1:179,437,578 | G/A | — | uncertain significance |
| rs755138451 | 1:179,437,596 | C/T | — | uncertain significance |
| rs199661575 | 1:179,437,707 | A/G | — | uncertain significance |
| rs6678546 | 1:179,448,853 | G/A | intron variant | — |
| rs752482764 | 1:179,452,273 | G/A | — | uncertain significance |
| rs368565108 | 1:179,452,316 | G/A | — | uncertain significance |
| rs769787722 | 1:179,452,333 | G/A | — | uncertain significance |
| rs56101948 | 1:179,459,061 | A/G | — | — |
| rs144846426 | 1:179,460,745 | G/A | — | uncertain significance |
| rs200985964 | 1:179,460,824 | C/T | — | uncertain significance |
| rs764614976 | 1:179,460,866 | T/C | — | uncertain significance |
| rs2527424147 | 1:179,462,010 | C/T | — | uncertain significance |
| rs202135298 | 1:179,462,017 | G/A | — | uncertain significance |
| rs2527425927 | 1:179,462,070 | A/G | — | uncertain significance |
| rs12047808 | 1:179,469,314 | A/G | intron variant | — |
| rs202143471 | 1:179,478,525 | G/A | — | likely benign |
| rs574429925 | 1:179,494,505 | G/A | — | likely benign |
| rs751349104 | 1:179,503,867 | A/G | — | uncertain significance |
| rs143297876 | 1:179,503,909 | A/G | — | uncertain significance |
| rs374779835 | 1:179,503,933 | C/A | — | uncertain significance |
| rs1482219302 | 1:179,503,944 | A/C | — | uncertain significance |
| rs750204100 | 1:179,503,963 | T/C | — | uncertain significance |
| rs758850607 | 1:179,503,982 | G/C | — | uncertain significance |
| rs778142614 | 1:179,503,993 | A/G | — | likely benign |
| rs754952987 | 1:179,504,046 | G/C | — | uncertain significance |
| rs1453848830 | 1:179,504,073 | A/G | — | likely benign |
| rs748895978 | 1:179,504,089 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.