Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "F"
361 to 370 of 433 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

361
FAT atypical cadherin 4
CDHF14, CDHR11, FAT-J, FATJ, HKLLS2, NBLA00548, VMLDS2
Bipolar disorder, Congenital anomalies of the kidney and urinary tract, Cerebrofacioarticular syndrome, Color vision deficiency, Coronary artery disease, Cystic kidney disease, Esophageal squamous cell carcinoma, Hennekam syndrome, Periventricular nodular heterotopia, Insomnia, Kidney disease, Major depressive disorder, Melanoma, Open angle glaucoma, Small vessel stroke
View all (3 more)

362
FAST kinase domains 1
-
Glaucoma

363
Frizzled class receptor 3
Fz-3
Arthrogryposis multiplex congenita, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Obstructive pulmonary disease, Hydrocephalus, Schizophrenia, Williams syndrome

364
F-box protein 31
FBX14, FBXO14, Fbx31, MRT45, pp2386
Nonsyndromic intellectual disability, Cerebral palsy, Ectopic thyroid tissue, Human immunodeficiency virus infection, Intellectual developmental disorder, Peripheral neuropathy

365
F-box and leucine rich repeat protein 18
Fbl18
Hepatocellular carcinoma, Metabolic syndrome, Psoriasis, Scoliosis, Diabetes mellitus, type 2

366
Fraser extracellular matrix complex subunit 1
FRASRS1
Alzheimer disease, Congenital anomalies of the kidney and urinary tract, Obstructive pulmonary disease, Renal agenesis, Cryptophthalmos syndrome, Fraser syndrome, Generalized anxiety disorder, Retinal detachment

367
Fuzzy planar cell polarity protein
CPLANE3, FY, NTD
Caudal regression syndrome, Desbuquois syndrome, Jeune thoracic dystrophy, Majewski syndrome, Neural tube defect

368
F-box protein 11
FBX11, IDDFBA, PRMT9, UBR6, UG063H01, VIT1
Alzheimer disease, Asthma, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Bipolar disorder, Lynch syndrome, Developmental disability, Diverticular disease, Insomnia, Intellectual developmental disorder dysmorphic behavioral, Intellectual developmental disorder, Major depressive disorder, Neurodevelopmental disorders, Non-specific syndromic intellectual disability
View all (6 more)

369
Formin homology 2 domain containing 3
CMH28, FHOS2, Formactin2
Alzheimer disease, Cardiomyopathy, Color vision deficiency, Dementia, Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Otosclerosis, Ovarian cancer, Periodontitis, Scoliosis, Spinal muscular atrophy

370
Flavin adenine dinucleotide synthetase 1
FAD1, FADS, LSMFLAD, PP591
Squamous cell carcinoma