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"
281 to 290 of 584 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

281
Flap structure-specific endonuclease 1
FEN-1, MF1, RAD2
Colorectal cancer, Colorectal neoplasms, Crohn disease, Non-immune hydrops fetalis, Inflammatory bowel disease, Lung neoplasms, Ulcerative colitis

282
FER tyrosine kinase
PPP1R74, TYK3, p94-Fer
Asthma, Coronary artery disease, Duane retraction syndrome, Dupuytren contracture, Major depressive disorder, Psoriasis, Psychiatric disorders, Respiratory system infectious disease, Schizophrenia, Hypertension

283
Fer3 like bHLH transcription factor
N-TWIST, NATO3, NTWIST, PTFB, bHLHa31
Amyotrophic lateral sclerosis, Aortic stenosis, Aortic valve disease, Asthma, Atrial fibrillation, Brain aneurysm, Cancer, Central nervous system cancer, Colorectal cancer, Coronary artery disease, Diabetes mellitus, Glioblastoma, Glioma, Heart failure, Major depressive disorder
View all (4 more)

284
FERM domain containing kindlin 1
C20orf42, DTGCU2, KIND1, UNC112A, URP1
Crohn disease, Inflammatory bowel disease, Kindler epidermolysis bullosa, Skin disease, Ulcerative colitis

285
FERM domain containing kindlin 2
KIND2, MIG2, PLEKHC1, UNC112, UNC112B, mig-2
Alzheimer disease, Angle closure glaucoma, Atrial fibrillation, Colonic neoplasms, Dementia, Dilated cardiomyopathy, Glaucoma, Hypertension, Hypertrophic cardiomyopathy, Open angle glaucoma, Primary angle closure glaucoma, Prostate cancer, Urinary bladder neoplasms

286
FERM domain containing kindlin 3
KIND3, MIG-2, MIG2B, UNC112C, URP2, URP2SF
Attention deficit hyperactivity disorder, Platelet disorder, Congenital leukocyte adherence deficiency, Desbuquois syndrome, Hemorrhage, Leukocyte adhesion deficiency, Major depressive disorder, Oligodendroglioma, Osteopetrosis, Uterine fibroid

287
FERRY endosomal RAB5 effector complex subunit 3
C12orf4, Fy-3, MRT66
Attention deficit hyperactivity disorder, Nonsyndromic intellectual disability, Intellectual developmental disorder, Diabetes mellitus type 2

288
FES proto-oncogene, tyrosine kinase
FPS
Androgenetic alopecia, Atrial fibrillation, Attention deficit hyperactivity disorder, Cardiovascular disease, Ischemic heart disease, Coronary artery disease, Diabetes mellitus, Hypertension, Insomnia, Myocardial infarction, Myocardial ischemia, Osteoarthritis, Post-traumatic stress disorder, Schizophrenia

289
FEV transcription factor, ETS family member
HSRNAFEV, PET-1
Autism, Major depressive disorder, Mood disorder, Myocardial ischemia

290
Fasciculation and elongation protein zeta 1
UNC-76
Alzheimer disease, Astrocytoma, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Major depressive disorder, Peripheral arterial disease, Psychotic disorders, Schizophrenia