Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4761 to 4770 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4761
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

4762
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

4763
FLYWCH-type zinc finger 1
-
Russell-silver syndrome, Sialolithiasis

4764
FLYWCH family member 2
-
Erythematosquamous dermatosis, Seborrheic dermatitis

4765
Formation of mitochondrial complex V assembly factor 1
C7orf55, HSPC268
Parkinson disease, Secondary parkinson disease, Schizophrenia, Usher syndrome

4766
FMC1-LUC7L2 readthrough
C7orf55, C7orf55-LUC7L2, FMC1
Asthma, Usher syndrome

4767
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

4768
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

4769
Formin like 1
C17orf1, C17orf1B, FHOD4, FMNL, KW-13
Asthma, Dementia, Hypothyroidism, Liver cirrhosis

4770
Formin like 2
FHOD2
Asthma, Astrocytoma, Barrett esophagus, Corneal astigmatism, Crohn disease, Esophageal adenocarcinoma, Glaucoma, Liver cirrhosis, Moyamoya disease, Open angle glaucoma, Oropharyngeal cancer, Diabetes mellitus type 2