Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4741 to 4750 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4741
FLYWCH-type zinc finger 1
-
Russell-silver syndrome, Sialolithiasis

4742
FLYWCH family member 2
-
Erythematosquamous dermatosis, Seborrheic dermatitis

4743
Formation of mitochondrial complex V assembly factor 1
C7orf55, HSPC268
Parkinson disease, Secondary parkinson disease, Schizophrenia, Usher syndrome

4744
FMC1-LUC7L2 readthrough
C7orf55, C7orf55-LUC7L2, FMC1
Asthma, Usher syndrome

4745
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

4746
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

4747
Formin like 1
C17orf1, C17orf1B, FHOD4, FMNL, KW-13
Asthma, Dementia, Hypothyroidism

4748
Formin like 2
FHOD2
Asthma, Astrocytoma, Barrett esophagus, Corneal astigmatism, Crohn disease, Esophageal adenocarcinoma, Glaucoma, Moyamoya disease, Open angle glaucoma, Oropharyngeal cancer, Diabetes mellitus type 2

4749
Flavin containing dimethylaniline monoxygenase 1
-
Amyotrophic lateral sclerosis, Autism, Motor neuron disease

4750
Flavin containing dimethylaniline monoxygenase 2
FMO1B1
Autism, Basal cell carcinoma, Endometriosis, Hyperopia