Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "F"
291 to 300 of 584 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

291
Fasciculation and elongation protein zeta 2
HUM3CL
Diverticular disease, Hemorrhoid, Metabolic syndrome, Myocardial ischemia, Diabetes mellitus type 2

292
FEZ family zinc finger 1
FEZ, HH22, ZNF312B
Attention deficit hyperactivity disorder, Breast cancer, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Oligodendroglioma, Osteoarthritis, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Schizophrenia, Sheehan syndrome, Substance abuse

293
FEZ family zinc finger 2
FEZ, FEZL, FKSG36, TOF, ZFP312, ZNF312
Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Psoriasis

294
Free fatty acid receptor 1
FFA1R, GPCR40, GPR40
Diabetes mellitus type 2

295
Free fatty acid receptor 2
FFA2R, GPR43
Appendicitis, Bipolar disorder, Central nervous system cancer, Disorder of appendix, Hypertension, Glioblastoma, Glioma

296
Free fatty acid receptor 3
FFA3R, GPR41, GPR42
Hypertension

297
Free fatty acid receptor 4
BMIQ10, GPR120, GPR129, GT01, O3FAR1, OB10Q, PGR4
Body mass index, Colorectal cancer

298
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)

299
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)

300
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