DNER
delta/notch like EGF repeat containing
Summary
Predicted to enable Notch binding activity. Involved in central nervous system development. Located in dendrite; early endosome; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2469663723 | 2:230,223,345 | C/T | — | uncertain significance |
| rs7594321 | 2:230,224,031 | T/C | intron variant | — |
| rs111685443 | 2:230,231,597 | C/T | — | benign |
| rs143853534 | 2:230,231,598 | C/T | — | uncertain significance |
| rs767646633 | 2:230,231,746 | C/T | — | uncertain significance |
| rs1692367406 | 2:230,231,800 | G/A | — | uncertain significance |
| rs149348216 | 2:230,231,812 | T/C | — | likely benign |
| rs142994637 | 2:230,231,819 | G/A | — | benign |
| rs147002066 | 2:230,231,828 | T/C | — | benign |
| rs751919113 | 2:230,271,972 | A/G | — | uncertain significance |
| rs200801433 | 2:230,271,991 | G/A | — | benign |
| rs6712150 | 2:230,279,522 | G/A | intron variant | — |
| rs199948718 | 2:230,282,859 | T/C | — | uncertain significance |
| rs138126887 | 2:230,284,607 | T/C | intron variant | — |
| rs7571817 | 2:230,291,975 | G/A | intron variant | — |
| rs111868934 | 2:230,307,821 | A/T | intron variant | — |
| rs1331261511 | 2:230,312,044 | G/A | — | uncertain significance |
| rs372420000 | 2:230,312,070 | C/T | — | uncertain significance |
| rs144811178 | 2:230,312,075 | C/T | — | likely benign |
| rs1478710470 | 2:230,312,086 | C/A | — | uncertain significance |
| rs767590493 | 2:230,312,173 | C/T | — | uncertain significance |
| rs140576705 | 2:230,312,216 | G/A | — | benign |
| rs772338273 | 2:230,312,224 | C/T | — | uncertain significance |
| rs747200067 | 2:230,341,886 | G/C | — | uncertain significance |
| rs774000987 | 2:230,341,937 | C/T | — | uncertain significance |
| rs2469829517 | 2:230,341,942 | T/C | — | uncertain significance |
| rs11890081 | 2:230,349,989 | T/G | — | — |
| rs376161329 | 2:230,377,558 | C/T | — | uncertain significance |
| rs369585918 | 2:230,377,561 | G/A | — | uncertain significance |
| rs765060539 | 2:230,377,562 | C/T | — | uncertain significance |
| rs751461005 | 2:230,377,585 | T/G | — | uncertain significance |
| rs779246523 | 2:230,377,600 | T/G | — | uncertain significance |
| rs2469879201 | 2:230,377,639 | C/A | — | uncertain significance |
| rs1455980332 | 2:230,377,648 | G/A | — | uncertain significance |
| rs780759032 | 2:230,411,670 | G/A | — | uncertain significance |
| rs146673499 | 2:230,411,712 | T/G | — | uncertain significance |
| rs150417576 | 2:230,411,766 | C/T | — | uncertain significance |
| rs181076796 | 2:230,431,615 | T/A | intron variant | — |
| rs762678520 | 2:230,453,122 | T/C | — | uncertain significance |
| rs146172282 | 2:230,453,140 | G/A | — | uncertain significance |
| rs373276946 | 2:230,453,150 | G/A | — | uncertain significance |
| rs149123458 | 2:230,453,153 | C/T | — | uncertain significance |
| rs200771367 | 2:230,453,157 | C/T | — | likely benign |
| rs757389003 | 2:230,453,177 | C/T | — | uncertain significance |
| rs371243645 | 2:230,453,214 | G/A | — | benign |
| rs146704189 | 2:230,456,341 | C/T | — | benign |
| rs755499578 | 2:230,456,370 | C/T | — | uncertain significance |
| rs202238472 | 2:230,456,379 | G/A | — | uncertain significance |
| rs1697609658 | 2:230,456,423 | A/C | — | uncertain significance |
| rs759503890 | 2:230,456,429 | C/T | — | uncertain significance |
| rs147533391 | 2:230,456,456 | G/A | — | benign |
| rs201766920 | 2:230,456,479 | C/G | — | uncertain significance |
| rs768586225 | 2:230,456,509 | A/C | — | uncertain significance |
| rs774350468 | 2:230,456,526 | A/C | — | uncertain significance |
| rs6705299 | 2:230,478,658 | C/A | — | — |
| rs1861612 | 2:230,522,398 | G/A | intron variant | — |
| rs1269905269 | 2:230,578,974 | C/G | — | uncertain significance |
| rs2469506148 | 2:230,579,052 | C/G | — | uncertain significance |
| rs954714895 | 2:230,579,117 | G/A | — | uncertain significance |
| rs2154217996 | 2:230,579,132 | G/A | — | uncertain significance |
| rs542077701 | 2:230,579,815 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.