Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4881 to 4890 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4881
Fascin actin-bundling protein 2, retinal
RFSN, RP30
Hearing loss, Leber congenital amaurosis, Macular degeneration, Meniere disease, Retinitis pigmentosa

4882
Fascin actin-bundling protein 3
-
Attention deficit hyperactivity disorder, Autism, Duodenal ulcer, Gestational diabetes, Hypospadias, Diabetes mellitus type 2

4883
Fibronectin type III and SPRY domain containing 1
GLFND, MIR1
Stomach neoplasms

4884
Fibronectin type III and SPRY domain containing 1 like
CCDC10, CSDUFD1, FSD1CL, FSD1NL, MIR1
Congenital hydrocephalus, Post-traumatic stress disorder

4885
Fibronectin type III and SPRY domain containing 2
SPRYD1
Colorectal adenoma, Diabetes mellitus type 2

4886
Follicle stimulating hormone subunit beta
HH24
Amenorrhea, Isolated follicle-stimulating hormone deficiency, Hypogonadism, Hypogonadotropic hypogonadism, Female infertility, Male infertility

4887
Follicle stimulating hormone receptor
FSHR1, FSHRO, LGR1, ODG1
46, xx gonadal dysgenesis, Erectile dysfunction, Gonadal dysgenesis, Ovarian dysgenesis, Ovarian hyperstimulation syndrome, Polycystic ovary syndrome, Prostate cancer

4888
Fibrous sheath interacting protein 1
HSD10
Asthma, Diverticular disease, Gout, Obesity, Squamous cell carcinoma

4889
Fibrous sheath interacting protein 2
SPGF34
Congenital impairment of spermatozoa motility, Spermatogenic failure

4890
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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