ADAM28
ADAM metallopeptidase domain 28
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 protein encoded by this gene is a lymphocyte-expressed ADAM protein. This gene is present in a gene cluster with other members of the ADAM family on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs375265578 | 8:24,157,490 | G/A | — | likely benign |
| rs144193683 | 8:24,168,880 | T/A | — | uncertain significance |
| rs936843897 | 8:24,168,947 | T/C | — | uncertain significance |
| rs886625998 | 8:24,170,906 | A/G | — | uncertain significance |
| rs2486760254 | 8:24,170,932 | T/C | — | uncertain significance |
| rs140230044 | 8:24,170,956 | C/A | — | benign |
| rs755646329 | 8:24,171,026 | G/A | — | uncertain significance |
| rs147092030 | 8:24,171,056 | T/G | — | uncertain significance |
| rs367907463 | 8:24,171,066 | C/G | — | uncertain significance |
| rs200839167 | 8:24,177,788 | A/G | — | uncertain significance |
| rs148324205 | 8:24,181,375 | C/T | — | uncertain significance |
| rs1285752340 | 8:24,181,386 | A/G | — | uncertain significance |
| rs2486939998 | 8:24,181,387 | T/C | — | uncertain significance |
| rs369442825 | 8:24,181,504 | C/T | — | uncertain significance |
| rs962801385 | 8:24,184,080 | G/T | — | likely benign |
| rs555577712 | 8:24,184,134 | G/A | — | uncertain significance |
| rs139736903 | 8:24,184,140 | G/A | — | likely benign |
| rs770708054 | 8:24,187,534 | A/T | — | uncertain significance |
| rs1324560118 | 8:24,187,549 | G/C | — | uncertain significance |
| rs568315585 | 8:24,188,668 | A/G | — | uncertain significance |
| rs760445061 | 8:24,188,669 | T/C | — | likely benign |
| rs1813309438 | 8:24,188,677 | C/T | — | uncertain significance |
| rs199891707 | 8:24,188,685 | A/G | — | uncertain significance |
| rs1338909579 | 8:24,188,695 | G/T | — | uncertain significance |
| rs142585876 | 8:24,188,832 | A/C | — | uncertain significance |
| rs762484740 | 8:24,190,179 | A/G | — | uncertain significance |
| rs2487116499 | 8:24,190,207 | G/A | — | uncertain significance |
| rs377002272 | 8:24,190,222 | C/G | — | likely benign |
| rs764292584 | 8:24,190,225 | T/G | — | uncertain significance |
| rs746405162 | 8:24,190,249 | G/T | — | uncertain significance |
| rs150239663 | 8:24,193,039 | T/C | — | likely benign |
| rs768568505 | 8:24,193,105 | G/A | — | uncertain significance |
| rs1366233563 | 8:24,193,152 | C/T | — | uncertain significance |
| rs2487230885 | 8:24,196,993 | G/T | — | uncertain significance |
| rs749570387 | 8:24,196,994 | A/G | — | uncertain significance |
| rs766324788 | 8:24,197,006 | A/G | — | uncertain significance |
| rs191658345 | 8:24,197,035 | G/T | — | uncertain significance |
| rs201643797 | 8:24,199,149 | C/G | — | affects |
| rs145453785 | 8:24,199,150 | G/A | — | likely benign |
| rs1814786824 | 8:24,199,208 | C/A | — | uncertain significance |
| rs985578168 | 8:24,201,030 | T/G | — | uncertain significance |
| rs754274112 | 8:24,201,070 | G/A | — | likely benign |
| rs1585718234 | 8:24,201,071 | A/G | — | uncertain significance |
| rs768784090 | 8:24,201,088 | G/A | — | uncertain significance |
| rs200346695 | 8:24,207,409 | A/G | — | likely benign |
| rs1267550203 | 8:24,207,464 | A/G | — | likely benign |
| rs556317287 | 8:24,208,746 | C/G | — | uncertain significance |
| rs2487419821 | 8:24,209,502 | G/A | — | uncertain significance |
| rs202242022 | 8:24,209,546 | A/G | — | uncertain significance |
| rs139099695 | 8:24,211,307 | C/T | — | likely benign |
| rs1816532682 | 8:24,211,912 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.