ADAMDEC1
ADAM like decysin 1
Summary
This encoded protein is thought to be a secreted protein belonging to the disintegrin metalloproteinase family. Its expression is upregulated during dendritic cells maturation. This protein may play an important role in dendritic cell function and their interactions with germinal center T cells. [provided by RefSeq, Jul 2008]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1441794912 | 8:24,242,049 | T/C | — | uncertain significance |
| rs2487517070 | 8:24,242,051 | G/A | — | uncertain significance |
| rs61731546 | 8:24,249,805 | C/T | — | benign |
| rs35372591 | 8:24,249,817 | T/C | — | uncertain significance |
| rs544795925 | 8:24,249,874 | C/T | — | uncertain significance |
| rs1339408966 | 8:24,249,885 | G/A | — | uncertain significance |
| rs77012108 | 8:24,250,809 | T/C | — | benign |
| rs779812850 | 8:24,251,583 | C/A | — | uncertain significance |
| rs369325197 | 8:24,251,614 | T/C | — | uncertain significance |
| rs7007084 | 8:24,251,659 | T/C | — | benign |
| rs201210348 | 8:24,253,290 | A/G | — | uncertain significance |
| rs148571165 | 8:24,253,302 | G/A | — | uncertain significance |
| rs750384295 | 8:24,254,847 | G/A | — | uncertain significance |
| rs766090181 | 8:24,254,854 | C/A | — | uncertain significance |
| rs200134300 | 8:24,254,856 | G/T | — | uncertain significance |
| rs1359549029 | 8:24,254,896 | A/G | — | uncertain significance |
| rs762810900 | 8:24,254,917 | C/T | — | uncertain significance |
| rs767394749 | 8:24,254,922 | G/A | — | likely benign |
| rs541880302 | 8:24,255,211 | C/T | — | uncertain significance |
| rs200386440 | 8:24,256,035 | G/A | — | uncertain significance |
| rs545416262 | 8:24,256,048 | T/C | — | uncertain significance |
| rs7004492 | 8:24,256,074 | T/C | — | benign |
| rs7001097 | 8:24,256,389 | A/T | — | benign |
| rs765908236 | 8:24,256,457 | A/G | — | uncertain significance |
| rs7005258 | 8:24,256,512 | T/C | — | benign |
| rs200469454 | 8:24,256,535 | A/G | — | uncertain significance |
| rs753778596 | 8:24,256,938 | T/C | — | uncertain significance |
| rs140087766 | 8:24,257,768 | A/T | — | uncertain significance |
| rs371112617 | 8:24,259,479 | A/C | — | uncertain significance |
| rs375249809 | 8:24,259,559 | A/T | — | uncertain significance |
| rs926178752 | 8:24,259,562 | A/G | — | uncertain significance |
| rs76707982 | 8:24,259,600 | C/T | — | benign |
| rs61731545 | 8:24,261,518 | G/A | — | benign |
| rs3765124 | 8:24,261,526 | A/G | missense variant | — |
| rs867548378 | 8:24,261,568 | C/A | — | uncertain significance |
| rs796298185 | 8:24,261,579 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.