DLGAP2
DLG associated protein 2
Summary
The product of this gene is a membrane-associated protein that may play a role in synapse organization and signalling in neuronal cells. This gene is biallelically expressed in the brain, however, only the paternal allele is expressed in the testis (PMID:18055845). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jun 2014]
Known Variants122 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs112628444 | 8:687,814 | G/T | — | benign |
| rs78256222 | 8:800,540 | T/C | intron variant | — |
| rs546907591 | 8:857,927 | C/T | — | likely benign |
| rs552498380 | 8:1,006,064 | A/G | — | — |
| rs146516733 | 8:1,024,996 | C/T | intron variant | — |
| rs12675046 | 8:1,030,133 | G/C | — | — |
| rs184480582 | 8:1,037,524 | A/G | intron variant | — |
| rs147358466 | 8:1,046,327 | G/A | regulatory region variant | — |
| rs7822264 | 8:1,098,386 | A/T | — | — |
| rs549237777 | 8:1,179,637 | T/A | — | — |
| rs982040763 | 8:1,208,864 | G/A | — | likely benign |
| rs17669535 | 8:1,244,224 | C/G | downstream gene variant | — |
| rs10101376 | 8:1,244,374 | G/A | coding sequence variant | — |
| rs10106591 | 8:1,328,238 | G/A | — | — |
| rs181281798 | 8:1,357,212 | G/T | intergenic variant | — |
| rs28680850 | 8:1,373,720 | G/A | intergenic variant | — |
| rs143620327 | 8:1,449,522 | G/C | — | likely benign |
| rs769477449 | 8:1,496,793 | C/T | — | likely benign |
| rs1269711770 | 8:1,496,965 | G/A | — | uncertain significance |
| rs776439807 | 8:1,497,026 | C/T | — | uncertain significance |
| rs374377737 | 8:1,497,040 | G/T | — | uncertain significance |
| rs1446141774 | 8:1,497,051 | G/T | — | uncertain significance |
| rs2485851087 | 8:1,497,080 | A/C | — | uncertain significance |
| rs759597316 | 8:1,497,128 | A/G | — | uncertain significance |
| rs770007555 | 8:1,497,130 | G/A | — | benign |
| rs760350104 | 8:1,497,139 | G/A | — | uncertain significance |
| rs2485851321 | 8:1,497,140 | A/G | — | uncertain significance |
| rs201415144 | 8:1,497,145 | T/C | — | uncertain significance |
| rs374898123 | 8:1,497,146 | G/T | — | uncertain significance |
| rs757352058 | 8:1,497,158 | A/C | — | uncertain significance |
| rs751956855 | 8:1,497,193 | C/G | — | uncertain significance |
| rs200052111 | 8:1,497,260 | G/A | — | benign |
| rs1331541047 | 8:1,497,353 | C/T | — | uncertain significance |
| rs1346091922 | 8:1,497,355 | C/G | — | uncertain significance |
| rs2130517378 | 8:1,497,398 | A/C | — | uncertain significance |
| rs746322363 | 8:1,497,424 | G/A | — | uncertain significance |
| rs2485852737 | 8:1,497,438 | G/A | — | likely benign |
| rs2485853157 | 8:1,497,541 | A/C | — | uncertain significance |
| rs1358754798 | 8:1,497,545 | A/G | — | uncertain significance |
| rs778052783 | 8:1,497,583 | C/A | — | uncertain significance |
| rs1304258576 | 8:1,497,585 | C/T | — | likely benign |
| rs765825782 | 8:1,497,617 | G/A | — | uncertain significance |
| rs376158978 | 8:1,497,659 | A/G | — | likely benign |
| rs1184349817 | 8:1,497,661 | G/A | — | uncertain significance |
| rs755154549 | 8:1,497,667 | A/G | — | uncertain significance |
| rs2485854241 | 8:1,497,704 | A/G | — | uncertain significance |
| rs2485854408 | 8:1,497,739 | C/A | — | uncertain significance |
| rs778714284 | 8:1,497,781 | C/G | — | uncertain significance |
| rs150999171 | 8:1,497,792 | C/G | — | benign |
| rs1417836296 | 8:1,497,795 | G/C | — | uncertain significance |
| rs1015888225 | 8:1,497,807 | C/G | — | uncertain significance |
| rs769129102 | 8:1,497,820 | C/G | — | uncertain significance |
| rs1182052906 | 8:1,497,823 | G/A | — | uncertain significance |
| rs370722015 | 8:1,513,839 | C/G | — | likely benign |
| rs2301963 | 8:1,514,009 | C/A | — | benign |
| rs1400249603 | 8:1,514,025 | G/T | — | uncertain significance |
| rs201868215 | 8:1,514,031 | C/T | — | likely benign |
| rs775353108 | 8:1,514,033 | G/A | — | uncertain significance |
| rs1971655 | 8:1,519,472 | C/G | — | — |
| rs201567259 | 8:1,574,930 | C/T | — | likely benign |
| rs761115101 | 8:1,574,937 | C/T | — | uncertain significance |
| rs762050332 | 8:1,575,045 | G/A | — | uncertain significance |
| rs1797683635 | 8:1,581,050 | G/C | — | uncertain significance |
| rs375507295 | 8:1,581,087 | C/T | — | uncertain significance |
| rs200490199 | 8:1,581,177 | C/T | — | uncertain significance |
| rs552932202 | 8:1,581,222 | C/T | — | likely benign |
| rs6995760 | 8:1,581,226 | A/G | — | benign |
| rs376920234 | 8:1,616,497 | G/A | — | conflicting classifications of pathogenicity |
| rs750898090 | 8:1,616,507 | C/A | — | uncertain significance |
| rs370388753 | 8:1,616,531 | C/T | — | uncertain significance |
| rs779245245 | 8:1,616,536 | C/T | — | uncertain significance |
| rs373089965 | 8:1,616,568 | G/C | — | likely benign |
| rs377576966 | 8:1,616,572 | A/T | — | uncertain significance |
| rs1279305799 | 8:1,616,597 | C/A | — | uncertain significance |
| rs1798601148 | 8:1,616,617 | A/T | — | uncertain significance |
| rs200214556 | 8:1,616,621 | G/A | — | likely benign |
| rs375612222 | 8:1,616,639 | C/T | — | uncertain significance |
| rs4565482 | 8:1,616,640 | A/G | — | benign |
| rs777261867 | 8:1,616,656 | C/T | — | uncertain significance |
| rs199785303 | 8:1,616,658 | C/T | — | benign |
| rs7463888 | 8:1,616,675 | C/T | — | likely benign |
| rs2235112 | 8:1,616,718 | A/G | — | benign |
| rs764292335 | 8:1,616,720 | C/T | — | uncertain significance |
| rs369795477 | 8:1,616,768 | G/A | — | uncertain significance |
| rs201721317 | 8:1,616,771 | C/G | — | uncertain significance |
| rs774320515 | 8:1,616,774 | G/T | — | uncertain significance |
| rs377476569 | 8:1,616,776 | G/C | — | uncertain significance |
| rs1798609316 | 8:1,616,812 | C/T | — | uncertain significance |
| rs535837045 | 8:1,616,822 | G/A | — | likely benign |
| rs1012436728 | 8:1,616,836 | G/A | — | uncertain significance |
| rs2235113 | 8:1,616,863 | C/G | — | benign |
| rs754192203 | 8:1,617,959 | C/T | — | likely benign |
| rs369578407 | 8:1,624,736 | G/A | — | uncertain significance |
| rs904926499 | 8:1,624,741 | C/T | — | uncertain significance |
| rs555422589 | 8:1,624,742 | G/T | — | uncertain significance |
| rs2486191135 | 8:1,624,744 | G/A | — | uncertain significance |
| rs2486195488 | 8:1,626,390 | T/G | — | uncertain significance |
| rs149482724 | 8:1,626,467 | G/A | — | benign |
| rs1450874518 | 8:1,626,555 | C/T | — | uncertain significance |
| rs765947691 | 8:1,626,556 | G/A | — | uncertain significance |
Showing 100 of 122 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.