Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "F"
291 to 300 of 580 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

291
Free fatty acid receptor 1
FFA1R, GPCR40, GPR40
Diabetes mellitus type 2

292
Free fatty acid receptor 2
FFA2R, GPR43
Appendicitis, Bipolar disorder, Central nervous system cancer, Appendiceal disorder, Hypertension, Glioblastoma, Glioma

293
Free fatty acid receptor 3
FFA3R, GPR41, GPR42
Hypertension

294
Free fatty acid receptor 4
BMIQ10, GPR120, GPR129, GT01, O3FAR1, OB10Q, PGR4
Body mass index, Colorectal cancer

295
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
View all (7 more)

296
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
View all (6 more)

297
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

298
FYVE, RhoGEF and PH domain containing 2
ZFYVE4
Colonic neoplasms, Hypothyroidism, Ovarian cysts

299
FYVE, RhoGEF and PH domain containing 3
ZFYVE5
Myocardial infarction

300
FYVE, RhoGEF and PH domain containing 4
CMT4H, FRABP, ZFYVE6
Cerebral atherosclerosis, Charcot-marie-tooth disease, Dejerine-sottas disease, Hereditary motor and sensory neuropathies, Hypertension, Hypertrophic neuropathy, Parkinson disease, Peripheral neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome