DLGAP5
DLG associated protein 5
Summary
Predicted to enable microtubule binding activity. Predicted to be involved in several processes, including centrosome localization; kinetochore assembly; and mitotic spindle organization. Located in cytosol; nucleus; and spindle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2274273 | 14:55,614,636 | G/A | downstream gene variant | — |
| rs368350454 | 14:55,617,540 | T/C | — | uncertain significance |
| rs866588854 | 14:55,618,431 | T/C | — | uncertain significance |
| rs749828854 | 14:55,618,481 | C/T | — | uncertain significance |
| rs147229036 | 14:55,618,518 | T/C | — | uncertain significance |
| rs2504986821 | 14:55,618,546 | A/C | — | uncertain significance |
| rs2504986988 | 14:55,618,625 | A/G | — | uncertain significance |
| rs1882034570 | 14:55,618,659 | C/T | — | uncertain significance |
| rs142873440 | 14:55,621,357 | A/T | — | uncertain significance |
| rs573867710 | 14:55,621,386 | G/A | — | uncertain significance |
| rs771030717 | 14:55,621,410 | G/A | — | uncertain significance |
| rs753319263 | 14:55,621,455 | G/C | — | uncertain significance |
| rs778417884 | 14:55,621,467 | T/C | — | likely benign |
| rs1341446458 | 14:55,625,339 | A/G | — | uncertain significance |
| rs776508223 | 14:55,625,355 | T/A | — | uncertain significance |
| rs767025301 | 14:55,625,378 | T/C | — | uncertain significance |
| rs372884646 | 14:55,625,389 | C/T | — | uncertain significance |
| rs770096204 | 14:55,629,787 | C/T | — | uncertain significance |
| rs982757666 | 14:55,636,206 | C/G | — | uncertain significance |
| rs6650508 | 14:55,636,595 | A/G | intron variant | — |
| rs80024343 | 14:55,637,459 | C/G | — | uncertain significance |
| rs2505008065 | 14:55,637,488 | T/A | — | uncertain significance |
| rs11845848 | 14:55,638,701 | T/G | intron variant | — |
| rs369345355 | 14:55,642,077 | C/T | — | uncertain significance |
| rs377026946 | 14:55,642,100 | C/T | — | likely benign |
| rs2505013571 | 14:55,642,122 | A/G | — | likely benign |
| rs1359390059 | 14:55,642,182 | A/C | — | uncertain significance |
| rs140578230 | 14:55,642,188 | G/C | — | uncertain significance |
| rs552310872 | 14:55,642,647 | G/A | — | uncertain significance |
| rs199582303 | 14:55,642,667 | C/G | — | likely benign |
| rs2505014808 | 14:55,642,705 | C/T | — | uncertain significance |
| rs72718819 | 14:55,643,773 | T/G | — | benign |
| rs1350225677 | 14:55,643,799 | T/C | — | uncertain significance |
| rs1883094928 | 14:55,643,805 | T/A | — | uncertain significance |
| rs139172891 | 14:55,643,828 | T/C | — | uncertain significance |
| rs1416947943 | 14:55,643,832 | C/T | — | uncertain significance |
| rs372754218 | 14:55,643,847 | T/A | — | uncertain significance |
| rs1446004516 | 14:55,644,015 | T/C | — | likely benign |
| rs368885720 | 14:55,646,352 | C/T | — | uncertain significance |
| rs532075792 | 14:55,647,419 | C/T | — | uncertain significance |
| rs372697699 | 14:55,647,424 | C/T | — | uncertain significance |
| rs200979225 | 14:55,647,457 | C/T | — | uncertain significance |
| rs754962532 | 14:55,647,464 | T/G | — | uncertain significance |
| rs143819646 | 14:55,647,982 | G/A | — | uncertain significance |
| rs2505021357 | 14:55,647,991 | C/T | — | uncertain significance |
| rs369464956 | 14:55,650,345 | C/T | — | uncertain significance |
| rs748593016 | 14:55,650,378 | T/C | — | uncertain significance |
| rs145728451 | 14:55,650,390 | T/G | — | uncertain significance |
| rs750038944 | 14:55,650,454 | G/C | — | uncertain significance |
| rs7147106 | 14:55,652,189 | G/C | — | — |
| rs1451886728 | 14:55,655,752 | T/A | — | uncertain significance |
| rs757766430 | 14:55,655,761 | C/G | — | uncertain significance |
| rs372521527 | 14:55,655,776 | C/T | — | uncertain significance |
| rs747869629 | 14:55,655,830 | A/C | — | uncertain significance |
| rs201234769 | 14:55,655,872 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.