FNBP1
formin binding protein 1
Summary
The protein encoded by this gene is a member of the formin-binding-protein family. The protein contains an N-terminal Fer/Cdc42-interacting protein 4 (CIP4) homology (FCH) domain followed by a coiled-coil domain, a proline-rich motif, a second coiled-coil domain, a Rho family protein-binding domain (RBD), and a C-terminal SH3 domain. This protein binds sorting nexin 2 (SNX2), tankyrase (TNKS), and dynamin; an interaction between this protein and formin has not been demonstrated yet in human. [provided by RefSeq, Jul 2008]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs544636539 | 9:132,658,175 | A/T | — | uncertain significance |
| rs369400982 | 9:132,658,192 | T/C | — | uncertain significance |
| rs753782222 | 9:132,658,194 | C/T | — | uncertain significance |
| rs747213580 | 9:132,658,252 | C/T | — | uncertain significance |
| rs138991769 | 9:132,662,311 | G/A | — | benign |
| rs759041250 | 9:132,662,321 | G/A | — | uncertain significance |
| rs1184132946 | 9:132,662,370 | T/C | — | uncertain significance |
| rs200153012 | 9:132,662,721 | C/T | — | uncertain significance |
| rs2036696798 | 9:132,662,738 | G/A | — | uncertain significance |
| rs367878072 | 9:132,662,790 | G/A | — | uncertain significance |
| rs111319812 | 9:132,662,825 | G/C | — | benign |
| rs2491350827 | 9:132,665,201 | C/T | — | likely benign |
| rs776554206 | 9:132,665,228 | C/T | — | uncertain significance |
| rs757294604 | 9:132,671,268 | G/A | — | uncertain significance |
| rs371128214 | 9:132,671,269 | G/A | — | uncertain significance |
| rs374120316 | 9:132,671,270 | T/C | — | likely benign |
| rs775287536 | 9:132,686,176 | C/T | — | uncertain significance |
| rs578112983 | 9:132,686,185 | G/A | — | uncertain significance |
| rs200818836 | 9:132,686,256 | G/T | — | uncertain significance |
| rs780787179 | 9:132,686,262 | G/T | — | uncertain significance |
| rs2492530971 | 9:132,686,302 | T/A | — | uncertain significance |
| rs199797411 | 9:132,687,279 | T/C | — | uncertain significance |
| rs2492605463 | 9:132,687,288 | A/G | — | uncertain significance |
| rs777423514 | 9:132,687,310 | C/T | — | uncertain significance |
| rs2492771327 | 9:132,689,584 | T/G | — | uncertain significance |
| rs753490934 | 9:132,689,599 | T/C | — | uncertain significance |
| rs2492922418 | 9:132,691,949 | T/C | — | uncertain significance |
| rs113054539 | 9:132,719,371 | C/A | regulatory region variant | — |
| rs761422735 | 9:132,719,722 | C/T | — | uncertain significance |
| rs1229484923 | 9:132,720,794 | C/A | — | uncertain significance |
| rs1172028999 | 9:132,740,775 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.