ADAM21
ADAM metallopeptidase domain 21
Summary
This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The expression of this gene expression is testis-specific. [provided by RefSeq, May 2011]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3751521 | 14:70,924,249 | A/G | synonymous variant | — |
| rs746044901 | 14:70,924,356 | A/C | — | uncertain significance |
| rs1215045822 | 14:70,924,359 | T/A | — | uncertain significance |
| rs139600813 | 14:70,924,364 | A/G | — | uncertain significance |
| rs150381704 | 14:70,924,433 | G/A | — | likely benign |
| rs773176656 | 14:70,924,614 | G/A | — | likely benign |
| rs538489673 | 14:70,924,728 | T/C | — | uncertain significance |
| rs143022031 | 14:70,924,754 | G/A | — | likely benign |
| rs780020827 | 14:70,924,951 | G/A | — | likely benign |
| rs761014608 | 14:70,924,989 | T/C | — | uncertain significance |
| rs1398089903 | 14:70,925,043 | T/G | — | uncertain significance |
| rs2504661890 | 14:70,925,068 | A/T | — | uncertain significance |
| rs766109818 | 14:70,925,106 | T/C | — | uncertain significance |
| rs182555358 | 14:70,925,111 | A/G | — | uncertain significance |
| rs1594983570 | 14:70,925,112 | T/C | — | uncertain significance |
| rs150695062 | 14:70,925,124 | T/G | — | uncertain significance |
| rs778028003 | 14:70,925,139 | G/T | — | uncertain significance |
| rs1259634123 | 14:70,925,165 | C/T | — | uncertain significance |
| rs371221473 | 14:70,925,268 | A/G | — | uncertain significance |
| rs1882466241 | 14:70,925,373 | C/G | — | uncertain significance |
| rs2504662566 | 14:70,925,432 | C/G | — | uncertain significance |
| rs775142915 | 14:70,925,439 | G/A | — | uncertain significance |
| rs1201806743 | 14:70,925,535 | T/C | — | uncertain significance |
| rs747032678 | 14:70,925,669 | C/T | — | uncertain significance |
| rs765852664 | 14:70,925,714 | G/T | — | uncertain significance |
| rs138163438 | 14:70,925,720 | T/C | — | uncertain significance |
| rs143741959 | 14:70,925,736 | G/A | — | uncertain significance |
| rs185589078 | 14:70,925,831 | C/A | — | uncertain significance |
| rs369445961 | 14:70,925,832 | G/A | — | uncertain significance |
| rs756059611 | 14:70,925,887 | T/G | — | uncertain significance |
| rs61979128 | 14:70,925,926 | C/A | — | uncertain significance |
| rs747464512 | 14:70,925,927 | A/T | — | uncertain significance |
| rs1429563514 | 14:70,925,933 | C/G | — | uncertain significance |
| rs778216803 | 14:70,925,991 | G/A | — | uncertain significance |
| rs1167953219 | 14:70,926,039 | A/G | — | uncertain significance |
| rs140682659 | 14:70,926,050 | G/C | — | uncertain significance |
| rs765176938 | 14:70,926,063 | G/A | — | uncertain significance |
| rs151162402 | 14:70,926,135 | A/G | — | uncertain significance |
| rs765290008 | 14:70,926,147 | T/G | — | uncertain significance |
| rs150287047 | 14:70,926,257 | G/A | — | likely benign |
| rs769600234 | 14:70,926,270 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.