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"
401 to 410 of 584 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

401
Fms related receptor tyrosine kinase 3 ligand
FL, FLG3L, FLT3L, IMD125
Central nervous system cancer, Glioblastoma, Glioma, Immunodeficiency

402
Fms related receptor tyrosine kinase 4
CHTD7, FLT-4, FLT41, LMPH1A, LMPHM1, PCL, VEGFR-3, VEGFR3
Capillary infantile hemangioma, Renal cell carcinoma, Congenital heart disease, Dementia, Non-immune hydrops fetalis, Lymphatic malformation, Lymphedema, Polycystic ovary syndrome, Tetralogy of fallot

403
FLVCR choline and heme transporter 1
AXPC1, FLVCR, MFSD7B, NEDMISH, PCA, PCARP, RETSNS, SLC49A1
Asthma, Hepatocellular carcinoma, Hereditary sensory and autonomic neuropathy, Jeune thoracic dystrophy, Neurodevelopmental disorder, Posterior column ataxia with retinitis pigmentosa, Retinitis pigmentosa, Retinopathy-sensory neuropathy syndrome, Sensory neuropathy, Short rib dysplasia-polydactyly syndrome, Stargardt disease

404
FLVCR choline and putative heme transporter 2
C14orf58, CCT, EPV, FLVCRL14q, MFSD7C, PVHH, SLC49A2
Byzanthine arch palate, Contracture of multiple joints, Encephaloclastic proliferative vasculopathy, Hydrops fetalis, Posterior column ataxia with retinitis pigmentosa, Ventricular septal defect

405
FLYWCH-type zinc finger 1
-
Russell-silver syndrome, Sialolithiasis

406
FLYWCH family member 2
-
Erythematosquamous dermatosis, Seborrheic dermatitis

407
Formation of mitochondrial complex V assembly factor 1
C7orf55, HSPC268
Parkinson disease, Secondary parkinson disease, Schizophrenia, Usher syndrome

408
FMC1-LUC7L2 readthrough
C7orf55, C7orf55-LUC7L2, FMC1
Asthma, Usher syndrome

409
Formin 1
FMN, LD
Alzheimer disease, Androgenetic alopecia, Colorectal adenoma, Colorectal cancer, Melanoma, Desbuquois syndrome, Gout, Major depressive disorder, Orofacial cleft, Perinatal disease, Prostate cancer, Urinary bladder cancer

410
Formin 2
-
Alzheimer disease, Nonsyndromic intellectual disability, Bone disease, Bone fracture, Bullous pemphigoid, Renal cell carcinoma, Carotid atherosclerosis, Colorectal cancer, Coronary artery disease, Dupuytren contracture, Hirschsprung disease, Hypothyroidism, Intellectual developmental disorder, Oligodendroglioma, Schizophrenia