CADM1
cell adhesion molecule 1
Summary
Enables signaling receptor binding activity. Involved in several processes, including cell recognition; positive regulation of cytokine production; and susceptibility to natural killer cell mediated cytotoxicity. Located in plasma membrane. Implicated in breast carcinoma and prostate cancer. Biomarker of cervix uteri carcinoma in situ. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1191208990 | 11:115,049,386 | C/T | — | likely benign |
| rs141386367 | 11:115,049,401 | C/G | — | uncertain significance |
| rs757194461 | 11:115,049,434 | G/C | — | likely benign |
| rs1012431388 | 11:115,049,450 | G/A | — | uncertain significance |
| rs11215403 | 11:115,058,585 | G/A | intron variant | — |
| rs141892754 | 11:115,080,365 | G/A | — | likely benign |
| rs983554177 | 11:115,080,382 | A/G | — | likely benign |
| rs139604912 | 11:115,085,401 | A/G | — | benign |
| rs34106103 | 11:115,085,419 | A/G | — | benign |
| rs374153035 | 11:115,085,424 | T/A | — | uncertain significance |
| rs779875593 | 11:115,085,451 | C/T | — | uncertain significance |
| rs770714520 | 11:115,088,623 | G/T | — | likely benign |
| rs113893105 | 11:115,088,647 | T/C | — | benign |
| rs551139124 | 11:115,088,649 | C/T | — | uncertain significance |
| rs377460211 | 11:115,088,662 | G/A | — | likely benign |
| rs145894931 | 11:115,088,683 | A/C | — | likely benign |
| rs146619481 | 11:115,088,717 | T/G | — | benign |
| rs4936323 | 11:115,091,119 | T/A | — | — |
| rs6589488 | 11:115,096,956 | A/G | — | — |
| rs138595924 | 11:115,099,876 | C/T | — | benign |
| rs12276946 | 11:115,099,995 | G/A | — | benign |
| rs758401125 | 11:115,102,091 | C/G | — | uncertain significance |
| rs756584318 | 11:115,102,106 | T/G | — | uncertain significance |
| rs201626870 | 11:115,102,168 | G/A | — | uncertain significance |
| rs768807528 | 11:115,102,201 | C/T | — | uncertain significance |
| rs10458966 | 11:115,102,758 | T/C | intron variant | — |
| rs1011065854 | 11:115,109,298 | T/G | — | uncertain significance |
| rs2496929242 | 11:115,109,321 | T/G | — | uncertain significance |
| rs2496939807 | 11:115,111,057 | C/G | — | uncertain significance |
| rs7950069 | 11:115,140,553 | G/A | intron variant | — |
| rs141836498 | 11:115,229,534 | G/A | upstream gene variant | — |
| rs11608105 | 11:115,251,190 | C/T | downstream gene variant | — |
| rs220842 | 11:115,282,172 | A/T | intron variant | — |
| rs220836 | 11:115,301,871 | C/G | — | — |
| rs17523342 | 11:115,311,131 | T/C | intron variant | — |
| rs220839 | 11:115,319,096 | A/G | — | — |
| rs766154073 | 11:115,374,991 | G/C | — | uncertain significance |
| rs751314966 | 11:115,374,996 | G/C | — | uncertain significance |
| rs777473830 | 11:115,375,013 | A/C | — | uncertain significance |
| rs45514793 | 11:115,375,101 | T/C | — | benign |
| rs752658601 | 11:115,375,102 | A/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.