Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "F"
331 to 340 of 433 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

331
Follistatin like 5
-
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cataract, Cerebral amyloid angiopathy, Dementia, Bipolar depression, Diabetic neuropathy, Diabetic retinopathy, Diverticular disease, Gastroenteritis, Leprosy, Major depressive disorder, Metabolic syndrome
View all (6 more)

332
Fem-1 homolog C
EUROIMAGE686608, EUROIMAGE783647, FEM1A
Asthma, Neurodevelopmental disorder, Conotruncal cardiac defect, Neurodevelopmental disorders, Non-specific syndromic intellectual disability

333
FAM20C golgi associated secretory pathway kinase
DMP-4, DMP4, G-CK, GEF-CK, RNS
Alzheimer disease, Amelogenesis imperfecta, Color vision deficiency, Desbuquois syndrome, Glioma

334
Fibrosin like 1
-
Aortic stenosis, Aortic valve disease, Atrial fibrillation, Basal cell carcinoma, Biliary tract cancer, Breast cancer, Cancer, Cardiovascular disease, Cervical cancer, Colorectal cancer, Neurodevelopmental disorder, Coronary artery disease, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer
View all (18 more)

335
FA complementation group M
FAAP250, KIAA1596, POF15, SPGF28
Aplastic anemia, Azoospermia, Central nervous system cancer, Fanconi anemia, Glioblastoma, Glioma, Hereditary breast cancer, Male infertility single gene azoospermia, Male infertility spermatogenesis disorder, Premature ovarian failure, Spermatogenic failure

336
FHF complex subunit HOOK interacting protein 2A
FAM160B1, KIAA1600, bA106M7.3
Alzheimer disease, Melanoma

337
FAST kinase domains 5
dJ1187M17.5
Schizophrenia

338
FKBP prolyl isomerase 10
BRKS, BRKS1, FKBP65, OI11, OI6, PPIASE, TLH1, hFKBP65
Arthrogryposis, Bone fragility with contractures, arterial rupture, and deafness, Bruck syndrome, Desbuquois syndrome, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome

339
FAM111 trypsin like peptidase A
GCLEB, KCS2
Kenny-caffey syndrome, Desbuquois syndrome, Osteocraniostenosis, Prostate cancer

340
Family with sequence similarity 217 member B
C20orf177, dJ551D2.5