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"
521 to 530 of 580 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

521
Fascin actin-bundling protein 3
-
Attention deficit hyperactivity disorder, Autism, Duodenal ulcer, Gestational diabetes, Hypospadias, Diabetes mellitus type 2

522
Fibronectin type III and SPRY domain containing 1
GLFND, MIR1
Stomach neoplasms

523
Fibronectin type III and SPRY domain containing 1 like
CCDC10, CSDUFD1, FSD1CL, FSD1NL, MIR1
Congenital hydrocephalus, Post-traumatic stress disorder

524
Fibronectin type III and SPRY domain containing 2
SPRYD1
Colorectal adenoma, Diabetes mellitus type 2

525
Follicle stimulating hormone subunit beta
HH24
Amenorrhea, Isolated follicle-stimulating hormone deficiency, Hypogonadism, Hypogonadotropic hypogonadism, Female infertility, Male infertility

526
Follicle stimulating hormone receptor
FSHR1, FSHRO, LGR1, ODG1
46,xy gonadal dysgenesis, Erectile dysfunction, Gonadal dysgenesis, Ovarian dysgenesis, Ovarian hyperstimulation syndrome, Polycystic ovary syndrome, Prostate cancer

527
Fibrous sheath interacting protein 1
HSD10
Asthma, Diverticular disease, Gout, Obesity, Squamous cell carcinoma

528
Fibrous sheath interacting protein 2
SPGF34
Congenital impairment of spermatozoa motility, Spermatogenic failure

529
Follistatin
FS
Alzheimer disease, Attention deficit hyperactivity disorder, Breast cancer, Breast neoplasms, Hepatocellular carcinoma, Color vision deficiency, Coronary artery disease, Gout, Hypertension, Keratoconus, Liver failure, Liver neoplasms, Metabolic syndrome, Orofacial cleft, Ovarian serous carcinoma
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530
Follistatin like 1
FRP, FSL1, MIR198, OCC-1, OCC1, tsc36
Aortic valve disease, Kidney failure, Schizophrenia, Scleroderma, Systemic sclerosis