CXADR
CXADR cell adhesion molecule
Summary
The protein encoded by this gene is a type I membrane receptor for group B coxsackieviruses and subgroup C adenoviruses. Several transcript variants encoding different isoforms have been found for this gene. Pseudogenes of this gene are found on chromosomes 15, 18, and 21. [provided by RefSeq, May 2011]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2060412142 | 21:18,885,472 | C/T | — | uncertain significance |
| rs2824337 | 21:18,905,398 | T/G | — | — |
| rs186722413 | 21:18,911,836 | G/C | intron variant | — |
| rs4818359 | 21:18,918,090 | G/T | — | — |
| rs768609263 | 21:18,919,438 | G/A | — | uncertain significance |
| rs755566570 | 21:18,919,443 | G/A | — | uncertain significance |
| rs749210959 | 21:18,919,456 | C/T | — | uncertain significance |
| rs2516535242 | 21:18,924,086 | A/G | — | uncertain significance |
| rs368675196 | 21:18,924,179 | C/T | — | uncertain significance |
| rs2516536319 | 21:18,924,205 | A/T | — | uncertain significance |
| rs770870922 | 21:18,924,213 | G/T | — | uncertain significance |
| rs1014268195 | 21:18,931,373 | A/C | — | uncertain significance |
| rs143991674 | 21:18,933,027 | T/A | — | benign |
| rs747606055 | 21:18,933,125 | G/C | — | uncertain significance |
| rs201624272 | 21:18,933,709 | C/G | — | uncertain significance |
| rs767607873 | 21:18,933,724 | C/T | — | uncertain significance |
| rs899509385 | 21:18,933,743 | G/A | — | likely benign |
| rs757637973 | 21:18,933,751 | C/T | — | uncertain significance |
| rs76877390 | 21:18,937,781 | C/T | — | uncertain significance |
| rs2516595614 | 21:18,937,782 | T/A | — | likely benign |
| rs765586953 | 21:18,937,797 | C/T | — | likely benign |
| rs372559893 | 21:18,937,798 | G/A | — | uncertain significance |
| rs1288477424 | 21:18,937,876 | C/T | — | uncertain significance |
| rs143764073 | 21:18,937,895 | G/A | — | uncertain significance |
| rs2516596680 | 21:18,937,914 | T/G | — | likely benign |
| rs200893570 | 21:18,937,973 | T/C | — | uncertain significance |
| rs752242351 | 21:18,937,993 | G/A | — | uncertain significance |
| rs760265761 | 21:18,937,995 | T/G | — | uncertain significance |
| rs753870489 | 21:18,938,000 | C/T | — | uncertain significance |
| rs2737872 | 21:18,940,479 | G/C | 3 prime UTR variant | — |
| rs12034 | 21:18,942,223 | G/A | 3 prime UTR variant | — |
| rs62239920 | 21:18,944,889 | G/C | — | — |
| rs2824372 | 21:18,947,037 | G/C | downstream gene variant | — |
| rs564747473 | 21:18,956,603 | G/A | — | — |
| rs530408688 | 21:18,976,221 | A/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.