FER
FER tyrosine kinase
Summary
The protein encoded by this gene is a member of the FPS/FES family of non-transmembrane receptor tyrosine kinases. It regulates cell-cell adhesion and mediates signaling from the cell surface to the cytoskeleton via growth factor receptors. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome X. [provided by RefSeq, Apr 2015]
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs79536589 | 5:108,084,113 | G/A | regulatory region variant | — |
| rs112949822 | 5:108,085,190 | G/A | regulatory region variant | — |
| rs113193866 | 5:108,086,710 | A/G | intron variant | — |
| rs112668446 | 5:108,090,134 | G/A | intron variant | — |
| rs71592765 | 5:108,091,000 | C/G | intron variant | — |
| rs79621178 | 5:108,091,191 | G/T | — | — |
| rs62361303 | 5:108,102,727 | C/A | — | — |
| rs4479887 | 5:108,110,324 | G/A | — | — |
| rs13177718 | 5:108,113,344 | C/T | intron variant | — |
| rs79409628 | 5:108,113,740 | G/T | intron variant | — |
| rs781096339 | 5:108,133,935 | C/A | — | uncertain significance |
| rs2532036664 | 5:108,133,938 | G/C | — | uncertain significance |
| rs56199104 | 5:108,134,072 | T/C | — | benign |
| rs6897572 | 5:108,141,110 | G/C | intron variant | — |
| rs2532275700 | 5:108,168,520 | A/G | — | uncertain significance |
| rs772795359 | 5:108,168,568 | T/C | — | uncertain significance |
| rs1482444077 | 5:108,168,586 | A/G | — | uncertain significance |
| rs1026316854 | 5:108,168,609 | G/C | — | uncertain significance |
| rs190406944 | 5:108,170,893 | C/G | upstream gene variant | — |
| rs55954478 | 5:108,171,483 | G/A | synonymous variant | — |
| rs5019041 | 5:108,179,863 | A/G | intron variant | — |
| rs10039951 | 5:108,190,727 | G/A | intron variant | — |
| rs35137434 | 5:108,191,383 | G/A | intron variant | — |
| rs138502993 | 5:108,203,512 | A/G | — | uncertain significance |
| rs915690711 | 5:108,207,073 | A/G | — | uncertain significance |
| rs2532589021 | 5:108,207,100 | A/C | — | uncertain significance |
| rs182613310 | 5:108,207,182 | A/G | — | uncertain significance |
| rs2532595697 | 5:108,207,804 | G/A | — | uncertain significance |
| rs149945605 | 5:108,207,912 | A/G | — | uncertain significance |
| rs6889995 | 5:108,210,304 | A/G | intron variant | — |
| rs1454761319 | 5:108,219,123 | T/C | — | uncertain significance |
| rs1765876266 | 5:108,219,201 | C/T | — | uncertain significance |
| rs75421844 | 5:108,220,554 | T/C | regulatory region variant | — |
| rs78962810 | 5:108,227,936 | C/T | downstream gene variant | — |
| rs34349846 | 5:108,229,418 | G/A | downstream gene variant | — |
| rs115520719 | 5:108,233,362 | T/C | — | benign |
| rs2532812145 | 5:108,233,535 | T/A | — | uncertain significance |
| rs758676832 | 5:108,281,845 | G/T | — | uncertain significance |
| rs775035329 | 5:108,290,475 | G/A | — | uncertain significance |
| rs2533337487 | 5:108,290,545 | T/G | — | uncertain significance |
| rs1758235617 | 5:108,290,589 | T/C | — | uncertain significance |
| rs147406165 | 5:108,290,629 | T/G | — | uncertain significance |
| rs34320303 | 5:108,294,949 | T/C | — | benign |
| rs937710904 | 5:108,294,974 | A/C | — | uncertain significance |
| rs1758847030 | 5:108,294,990 | C/G | — | uncertain significance |
| rs771260179 | 5:108,295,031 | C/G | — | uncertain significance |
| rs781568132 | 5:108,295,033 | G/T | — | likely benign |
| rs748902706 | 5:108,373,150 | G/A | — | uncertain significance |
| rs773762377 | 5:108,373,157 | T/C | — | likely benign |
| rs2534099165 | 5:108,382,858 | C/T | — | uncertain significance |
| rs2534099223 | 5:108,382,862 | A/C | — | uncertain significance |
| rs4957796 | 5:108,402,140 | T/C | intron variant | — |
| rs7710527 | 5:108,502,493 | G/A | intron variant | — |
| rs151332661 | 5:108,516,519 | G/A | — | uncertain significance |
| rs55876507 | 5:108,521,932 | C/T | — | benign |
| rs1582454977 | 5:108,523,151 | C/G | — | uncertain significance |
| rs149517787 | 5:108,523,190 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.