4651
|
|
|
FEZ family zinc finger 2 |
FEZ, FEZL, FKSG36, TOF, ZFP312, ZNF312 |
|
4652
|
|
|
Free fatty acid receptor 1 |
FFA1R, GPCR40, GPR40 |
|
4653
|
|
|
Free fatty acid receptor 2 |
FFA2R, GPR43 |
|
4654
|
|
|
Free fatty acid receptor 3 |
FFA3R, GPR41, GPR42 |
|
4655
|
|
|
Free fatty acid receptor 4 |
BMIQ10, GPR120, GPR129, GT01, O3FAR1, OB10Q, PGR4 |
|
4656
|
|
|
Fibrinogen alpha chain |
AMYLD2, Fib2 |
Amyloidosis, Cerebrovascular disorder, Cholelithiasis, Thromboembolic pulmonary hypertension, Congenital afibrinogenemia, Congenital fibrinogen deficiency, Congenital hypofibrinogenemia, Cor pulmonale, Deep vein thrombosis, Dysfibrinogenemia, Afibrinogenemia, Hypofibrinogenemia, Visceral amyloidosis, Heart disease, Kidney disease, Mouth neoplasms, Osteoporosis, Stroke, Thrombocytopenia, Thrombophilia, Thrombosis, Venous thromboembolismView all (7 more) |
4657
|
|
|
Fibrinogen beta chain |
HEL-S-78p |
Cardiovascular disease, Carotid artery disease, Ischemic heart disease, Obstructive pulmonary disease, Congenital afibrinogenemia, Congenital fibrinogen deficiency, Congenital hypofibrinogenemia, Coronary artery disease, Deep vein thrombosis, Dysfibrinogenemia, Afibrinogenemia, Hypofibrinogenemia, Kidney failure, Myocardial infarction, Myocardial ischemia, Osteoporosis, Parkinson disease, Stroke, Thrombocytopenia, Thrombophilia, Venous thromboembolismView all (6 more) |
4658
|
|
|
FYVE, RhoGEF and PH domain containing 1 |
AAS, FGDY, MRXS16, ZFYVE3 |
Aarskog-scott syndrome, x-linked, Attention deficit hyperactivity disorder, Congenital foot deformity, Congenital neurologic anomalies, Craniofacial abnormalities, Desbuquois syndrome, Growth disorder, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Urogenital abnormalities, X-linked intellectual disability |
4659
|
|
|
FYVE, RhoGEF and PH domain containing 2 |
ZFYVE4 |
|
4660
|
|
|
FYVE, RhoGEF and PH domain containing 3 |
ZFYVE5 |
|
