CDH22
cadherin 22
Summary
This gene is a member of the cadherin superfamily. The gene product is composed of five cadherin repeat domains and a cytoplasmic tail similar to the highly conserved cytoplasmic region of classical cadherins. Expressed predominantly in the brain, this putative calcium-dependent cell adhesion protein may play an important role in morphogenesis and tissue formation in neural and non-neural cells during development and maintenance of the brain and neuroendocrine organs. [provided by RefSeq, Jul 2008]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1013693322 | 20:44,803,153 | C/T | — | uncertain significance |
| rs747375025 | 20:44,803,168 | C/T | — | uncertain significance |
| rs766967938 | 20:44,803,174 | G/A | — | uncertain significance |
| rs1196868498 | 20:44,803,179 | C/A | — | uncertain significance |
| rs2085722215 | 20:44,803,269 | A/G | — | uncertain significance |
| rs747323649 | 20:44,803,270 | G/T | — | uncertain significance |
| rs58367300 | 20:44,803,287 | G/A | — | benign |
| rs369889875 | 20:44,803,344 | G/A | — | uncertain significance |
| rs2515748670 | 20:44,803,411 | C/G | — | uncertain significance |
| rs1256010062 | 20:44,803,479 | G/C | — | uncertain significance |
| rs1201138723 | 20:44,803,480 | C/G | — | uncertain significance |
| rs2515748920 | 20:44,803,482 | C/G | — | uncertain significance |
| rs1314733568 | 20:44,803,491 | G/C | — | uncertain significance |
| rs772485362 | 20:44,803,499 | G/C | — | likely benign |
| rs2515749036 | 20:44,803,501 | C/T | — | uncertain significance |
| rs1255677683 | 20:44,803,503 | G/C | — | uncertain significance |
| rs767171662 | 20:44,803,528 | C/T | — | uncertain significance |
| rs1358841223 | 20:44,803,529 | G/T | — | uncertain significance |
| rs555357889 | 20:44,803,579 | T/A | — | uncertain significance |
| rs2515749346 | 20:44,803,594 | T/C | — | uncertain significance |
| rs2515749431 | 20:44,803,629 | A/T | — | uncertain significance |
| rs760429162 | 20:44,803,657 | C/G | — | uncertain significance |
| rs73598378 | 20:44,806,628 | G/A | — | benign |
| rs751544343 | 20:44,806,631 | G/C | — | uncertain significance |
| rs764309034 | 20:44,806,737 | G/A | — | uncertain significance |
| rs771302958 | 20:44,806,807 | C/T | — | uncertain significance |
| rs1376910323 | 20:44,815,255 | G/T | — | uncertain significance |
| rs1476358793 | 20:44,815,500 | C/T | — | uncertain significance |
| rs892642938 | 20:44,815,569 | A/T | — | uncertain significance |
| rs2085938251 | 20:44,828,131 | C/T | — | uncertain significance |
| rs774418956 | 20:44,839,085 | C/T | — | likely benign |
| rs2515790438 | 20:44,839,165 | A/G | — | uncertain significance |
| rs765073257 | 20:44,839,183 | G/A | — | uncertain significance |
| rs750193948 | 20:44,839,184 | A/T | — | uncertain significance |
| rs146698097 | 20:44,841,696 | C/T | — | uncertain significance |
| rs749513480 | 20:44,845,516 | C/T | — | uncertain significance |
| rs753243077 | 20:44,845,568 | G/C | — | uncertain significance |
| rs368116505 | 20:44,869,716 | G/A | — | uncertain significance |
| rs758941722 | 20:44,869,746 | G/A | — | uncertain significance |
| rs771325273 | 20:44,879,818 | G/A | — | uncertain significance |
| rs1017987628 | 20:44,879,846 | G/T | — | uncertain significance |
| rs975011913 | 20:44,879,918 | C/T | — | uncertain significance |
| rs2425818 | 20:44,896,562 | A/G | intron variant | — |
| rs6065945 | 20:44,921,631 | C/G | regulatory region variant | — |
| rs536419192 | 20:44,936,607 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.