FAT2
FAT atypical cadherin 2
Summary
This gene is the second identified human homolog of the Drosophila fat gene, which encodes a tumor suppressor essential for controlling cell proliferation during Drosophila development. The gene product is a member of the cadherin superfamily, a group of integral membrane proteins characterized by the presence of cadherin-type repeats. In addition to containing 34 tandem cadherin-type repeats, the gene product has two epidermal growth factor (EGF)-like repeats and one laminin G domain. This protein most likely functions as a cell adhesion molecule, controlling cell proliferation and playing an important role in cerebellum development. [provided by RefSeq, Jul 2008]
Known Variants991 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs768452355 | 5:150,885,134 | T/C | — | uncertain significance |
| rs776323616 | 5:150,885,145 | C/T | — | likely benign |
| rs2480852078 | 5:150,885,173 | C/T | — | uncertain significance |
| rs781585839 | 5:150,885,181 | T/C | — | uncertain significance |
| rs756387333 | 5:150,885,187 | T/C | — | uncertain significance |
| rs746927092 | 5:150,885,207 | G/C | — | likely benign |
| rs570876522 | 5:150,885,217 | G/A | — | uncertain significance |
| rs538297256 | 5:150,885,218 | C/T | — | likely benign |
| rs2127562175 | 5:150,885,235 | A/T | — | uncertain significance |
| rs145577993 | 5:150,885,263 | C/T | — | conflicting classifications of pathogenicity |
| rs764570991 | 5:150,885,265 | C/T | — | uncertain significance |
| rs754066917 | 5:150,885,266 | G/A | — | uncertain significance |
| rs147369556 | 5:150,885,274 | C/T | — | uncertain significance |
| rs1445622376 | 5:150,885,275 | G/C | — | uncertain significance |
| rs1443089616 | 5:150,885,277 | A/G | — | uncertain significance |
| rs1235591397 | 5:150,885,295 | C/A | — | uncertain significance |
| rs199734683 | 5:150,885,299 | C/T | — | uncertain significance |
| rs371252623 | 5:150,885,310 | C/T | — | uncertain significance |
| rs149865780 | 5:150,885,322 | C/G | — | conflicting classifications of pathogenicity |
| rs754295945 | 5:150,885,323 | C/G | — | likely benign |
| rs2127562380 | 5:150,885,330 | C/T | — | likely benign |
| rs758351608 | 5:150,885,332 | G/A | — | uncertain significance |
| rs372063434 | 5:150,885,360 | C/T | — | likely benign |
| rs200478785 | 5:150,885,369 | A/G | — | likely benign |
| rs372212910 | 5:150,885,386 | C/T | — | uncertain significance |
| rs750561477 | 5:150,885,391 | C/T | — | conflicting classifications of pathogenicity |
| rs763266607 | 5:150,885,392 | G/A | — | uncertain significance |
| rs751686564 | 5:150,885,397 | C/T | — | uncertain significance |
| rs375536782 | 5:150,885,399 | G/C | — | likely benign |
| rs200172237 | 5:150,885,412 | C/T | — | uncertain significance |
| rs765038227 | 5:150,885,413 | G/A | — | uncertain significance |
| rs2480854274 | 5:150,885,425 | G/C | — | uncertain significance |
| rs144888662 | 5:150,885,451 | C/T | — | conflicting classifications of pathogenicity |
| rs769281607 | 5:150,885,452 | G/A | — | uncertain significance |
| rs1420405515 | 5:150,885,494 | A/G | — | uncertain significance |
| rs1321688494 | 5:150,885,510 | G/A | — | likely benign |
| rs1370186171 | 5:150,885,514 | C/G | — | uncertain significance |
| rs1253511727 | 5:150,885,529 | A/G | — | uncertain significance |
| rs202102338 | 5:150,885,550 | C/T | — | uncertain significance |
| rs148621159 | 5:150,885,551 | G/A | — | uncertain significance |
| rs112219343 | 5:150,885,558 | C/T | — | likely benign |
| rs142209223 | 5:150,885,564 | C/T | — | likely benign |
| rs775680918 | 5:150,885,565 | G/A | — | uncertain significance |
| rs765277888 | 5:150,885,587 | C/T | — | uncertain significance |
| rs146763283 | 5:150,885,612 | G/A | — | likely benign |
| rs778271634 | 5:150,885,638 | C/G | — | uncertain significance |
| rs771234278 | 5:150,885,640 | A/G | — | conflicting classifications of pathogenicity |
| rs750941139 | 5:150,885,660 | T/A | — | uncertain significance |
| rs165339 | 5:150,885,788 | G/T | — | benign |
| rs7723079 | 5:150,886,616 | G/A | — | benign |
| rs768734506 | 5:150,886,696 | C/T | — | likely benign |
| rs201787846 | 5:150,886,697 | G/A | — | benign |
| rs755091164 | 5:150,886,717 | A/G | — | uncertain significance |
| rs7723266 | 5:150,886,725 | G/A | — | benign |
| rs2480862005 | 5:150,886,741 | T/C | — | uncertain significance |
| rs111771262 | 5:150,886,764 | G/A | — | likely benign |
| rs750934872 | 5:150,886,766 | G/A | — | uncertain significance |
| rs145466001 | 5:150,886,768 | G/C | — | likely benign |
| rs780306307 | 5:150,886,772 | G/T | — | uncertain significance |
| rs1254003449 | 5:150,886,784 | G/T | — | uncertain significance |
| rs146563944 | 5:150,886,792 | C/G | — | uncertain significance |
| rs368309685 | 5:150,886,794 | G/C | — | likely benign |
| rs760355926 | 5:150,886,803 | A/G | — | likely benign |
| rs2480862660 | 5:150,886,813 | A/G | — | uncertain significance |
| rs543652342 | 5:150,886,819 | C/T | — | likely benign |
| rs144848990 | 5:150,886,820 | G/A | — | conflicting classifications of pathogenicity |
| rs1314096471 | 5:150,886,848 | G/A | — | likely benign |
| rs2480863042 | 5:150,886,865 | A/G | — | uncertain significance |
| rs755223311 | 5:150,886,876 | G/A | — | uncertain significance |
| rs1105168 | 5:150,886,882 | A/G | — | benign |
| rs748391997 | 5:150,886,883 | G/T | — | uncertain significance |
| rs1247771916 | 5:150,886,893 | G/T | — | uncertain significance |
| rs1363572881 | 5:150,886,895 | T/C | — | uncertain significance |
| rs1223774416 | 5:150,886,896 | G/A | — | likely benign |
| rs533240264 | 5:150,886,898 | T/C | — | benign |
| rs545597751 | 5:150,886,909 | G/A | — | uncertain significance |
| rs138705803 | 5:150,886,912 | C/T | — | conflicting classifications of pathogenicity |
| rs2480863766 | 5:150,886,918 | G/T | — | uncertain significance |
| rs367689507 | 5:150,886,928 | C/T | — | uncertain significance |
| rs1473131971 | 5:150,886,929 | G/A | — | likely benign |
| rs763502422 | 5:150,886,933 | G/T | — | uncertain significance |
| rs1457131869 | 5:150,886,949 | T/C | — | uncertain significance |
| rs752111755 | 5:150,886,952 | C/G | — | uncertain significance |
| rs779535153 | 5:150,886,968 | G/A | — | likely benign |
| rs1228781563 | 5:150,886,970 | C/T | — | uncertain significance |
| rs2480864635 | 5:150,886,981 | G/C | — | uncertain significance |
| rs1452825007 | 5:150,887,004 | G/A | — | likely benign |
| rs749389986 | 5:150,887,014 | C/G | — | uncertain significance |
| rs199556909 | 5:150,887,018 | G/A | — | uncertain significance |
| rs1448093304 | 5:150,887,020 | C/T | — | uncertain significance |
| rs1194173873 | 5:150,887,042 | C/T | — | likely benign |
| rs2127564796 | 5:150,887,057 | T/C | — | uncertain significance |
| rs767959528 | 5:150,887,062 | G/A | — | likely benign |
| rs143949083 | 5:150,887,066 | C/T | — | conflicting classifications of pathogenicity |
| rs760967696 | 5:150,887,067 | G/A | — | likely benign |
| rs201517523 | 5:150,887,069 | C/T | — | uncertain significance |
| rs1244384273 | 5:150,887,087 | A/G | — | likely benign |
| rs2127564903 | 5:150,887,103 | G/A | — | likely benign |
| rs528067490 | 5:150,887,108 | C/A | — | uncertain significance |
| rs201804836 | 5:150,887,109 | C/G | — | uncertain significance |
Showing 100 of 991 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.