FCHO2
FCH and mu domain containing endocytic adaptor 2
Summary
Enables identical protein binding activity. Involved in clathrin coat assembly and clathrin-dependent endocytosis. Located in clathrin-coated pit and clathrin-coated vesicle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2548332 | 5:72,255,610 | T/C | upstream gene variant | — |
| rs2545646 | 5:72,255,808 | T/A | — | — |
| rs62360742 | 5:72,268,545 | G/T | intron variant | — |
| rs150446942 | 5:72,268,547 | T/A | — | — |
| rs748139714 | 5:72,286,424 | A/G | — | uncertain significance |
| rs26578 | 5:72,300,463 | T/A | — | — |
| rs760036982 | 5:72,302,350 | G/A | — | uncertain significance |
| rs377489605 | 5:72,302,361 | G/A | — | uncertain significance |
| rs1249154250 | 5:72,311,538 | T/G | — | uncertain significance |
| rs751339379 | 5:72,311,543 | A/T | — | uncertain significance |
| rs531313433 | 5:72,313,056 | A/G | — | uncertain significance |
| rs1213229031 | 5:72,313,064 | T/C | — | uncertain significance |
| rs74290475 | 5:72,321,881 | C/A | — | — |
| rs114375833 | 5:72,333,010 | A/G | — | likely benign |
| rs377584362 | 5:72,333,030 | A/T | — | uncertain significance |
| rs30532 | 5:72,335,708 | C/G | — | — |
| rs62362193 | 5:72,345,509 | T/C | — | — |
| rs62362194 | 5:72,346,125 | T/C | intron variant | — |
| rs774230768 | 5:72,347,179 | A/T | — | uncertain significance |
| rs1369806910 | 5:72,348,209 | G/A | — | uncertain significance |
| rs369958358 | 5:72,350,364 | C/T | — | uncertain significance |
| rs1200503 | 5:72,351,062 | C/G | intron variant | — |
| rs166304 | 5:72,351,708 | T/A | intron variant | — |
| rs192247958 | 5:72,355,610 | G/C | intron variant | — |
| rs375969109 | 5:72,359,679 | A/G | — | uncertain significance |
| rs2478544468 | 5:72,359,743 | C/T | — | uncertain significance |
| rs201594850 | 5:72,364,508 | A/G | — | uncertain significance |
| rs369163520 | 5:72,364,538 | C/G | — | uncertain significance |
| rs764725301 | 5:72,364,541 | G/A | — | uncertain significance |
| rs470926 | 5:72,364,673 | A/G | intron variant | — |
| rs1010114140 | 5:72,370,578 | G/A | — | uncertain significance |
| rs775807760 | 5:72,374,040 | T/A | — | uncertain significance |
| rs2478619317 | 5:72,374,059 | G/A | — | uncertain significance |
| rs778923465 | 5:72,374,107 | T/G | — | uncertain significance |
| rs2478619535 | 5:72,374,111 | A/C | — | uncertain significance |
| rs1743099301 | 5:72,377,610 | G/A | — | uncertain significance |
| rs756769649 | 5:72,377,655 | T/C | — | uncertain significance |
| rs2478631225 | 5:72,377,767 | A/G | — | uncertain significance |
| rs147677243 | 5:72,383,471 | A/G | — | benign |
| rs2478647878 | 5:72,383,520 | G/A | — | uncertain significance |
| rs374987125 | 5:72,383,569 | G/A | — | uncertain significance |
| rs755196593 | 5:72,383,912 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.