DNAI3
dynein axonemal intermediate chain 3
Summary
Enables Arp2/3 complex binding activity. Involved in negative regulation of Arp2/3 complex-mediated actin nucleation and negative regulation of cell migration. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6695223 | 1:85,531,711 | C/G | — | — |
| rs148724953 | 1:85,537,631 | C/G | — | benign |
| rs373932758 | 1:85,537,681 | A/G | — | likely benign |
| rs370422920 | 1:85,546,977 | G/A | — | uncertain significance |
| rs201744091 | 1:85,546,984 | T/A | — | uncertain significance |
| rs776785603 | 1:85,547,006 | C/T | — | uncertain significance |
| rs752700346 | 1:85,547,034 | T/C | — | uncertain significance |
| rs12088304 | 1:85,547,050 | C/T | — | benign |
| rs745408608 | 1:85,547,078 | C/A | — | uncertain significance |
| rs1571163120 | 1:85,548,009 | T/C | — | likely benign |
| rs960822630 | 1:85,548,052 | A/G | — | uncertain significance |
| rs143362473 | 1:85,548,066 | G/T | — | uncertain significance |
| rs12029771 | 1:85,548,068 | G/A | — | uncertain significance |
| rs201360254 | 1:85,548,077 | A/T | — | uncertain significance |
| rs372052431 | 1:85,550,250 | C/G | — | uncertain significance |
| rs369105393 | 1:85,550,335 | A/G | — | uncertain significance |
| rs2526655309 | 1:85,550,344 | T/C | — | uncertain significance |
| rs1407286140 | 1:85,551,616 | G/C | — | uncertain significance |
| rs75414273 | 1:85,551,722 | G/A | — | benign |
| rs139516297 | 1:85,555,816 | C/G | — | uncertain significance |
| rs768234156 | 1:85,555,836 | A/G | — | uncertain significance |
| rs751633679 | 1:85,555,913 | A/G | — | uncertain significance |
| rs1185249183 | 1:85,559,151 | G/C | — | uncertain significance |
| rs761912893 | 1:85,559,174 | G/C | — | uncertain significance |
| rs138379333 | 1:85,559,205 | G/A | — | benign |
| rs544660942 | 1:85,559,287 | C/T | — | likely benign |
| rs753211625 | 1:85,560,141 | G/A | — | uncertain significance |
| rs1655072516 | 1:85,560,213 | G/C | — | uncertain significance |
| rs556050888 | 1:85,563,252 | A/C | — | uncertain significance |
| rs1165797017 | 1:85,563,260 | G/A | — | uncertain significance |
| rs370317049 | 1:85,563,282 | G/C | — | uncertain significance |
| rs1211843714 | 1:85,563,307 | G/A | — | uncertain significance |
| rs2526697077 | 1:85,563,316 | G/C | — | uncertain significance |
| rs192462237 | 1:85,563,344 | A/C | — | benign |
| rs374225786 | 1:85,564,236 | G/A | — | likely benign |
| rs1655196759 | 1:85,564,258 | A/G | — | uncertain significance |
| rs771327351 | 1:85,564,337 | T/C | — | uncertain significance |
| rs776721054 | 1:85,573,718 | C/T | — | uncertain significance |
| rs74095803 | 1:85,575,763 | C/T | — | benign |
| rs764622021 | 1:85,583,479 | T/G | — | uncertain significance |
| rs200763412 | 1:85,583,562 | T/C | intron variant | — |
| rs141934700 | 1:85,587,489 | G/A | — | uncertain significance |
| rs1450386366 | 1:85,587,507 | G/C | — | likely benign |
| rs755832945 | 1:85,589,819 | G/T | — | uncertain significance |
| rs1441431050 | 1:85,589,828 | C/G | — | uncertain significance |
| rs138281012 | 1:85,589,838 | C/T | — | benign |
| rs2526771330 | 1:85,589,840 | G/T | — | uncertain significance |
| rs549526220 | 1:85,589,849 | A/G | — | uncertain significance |
| rs1347262189 | 1:85,589,851 | A/T | — | uncertain significance |
| rs368100900 | 1:85,589,872 | T/A | — | uncertain significance |
| rs147802675 | 1:85,592,186 | G/T | — | benign |
| rs376740106 | 1:85,592,275 | T/G | — | uncertain significance |
| rs140671433 | 1:85,592,280 | C/T | — | benign |
| rs1656148690 | 1:85,592,285 | G/T | — | uncertain significance |
| rs79751387 | 1:85,592,334 | A/G | — | benign |
| rs138739634 | 1:85,592,336 | C/G | — | uncertain significance |
| rs17121810 | 1:85,594,437 | T/C | — | benign |
| rs17121837 | 1:85,595,714 | T/C | — | benign |
| rs2526787183 | 1:85,595,719 | A/G | — | uncertain significance |
| rs146618100 | 1:85,595,733 | C/T | — | uncertain significance |
| rs199645222 | 1:85,595,746 | G/A | — | uncertain significance |
| rs1197917813 | 1:85,595,760 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.