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"
161 to 170 of 584 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

161
FA complementation group B
FA2, FAAP90, FAAP95, FAB, FACB
Fanconi anemia, Intellectual developmental disorder, x-linked, Vacterl association, Vacterl-hydrocephalus syndrome

162
FA complementation group C
FA3, FAC, FACC
Atrial fibrillation, Color vision deficiency, Colorectal cancer, Congenital cardiovascular anomaly, Esophageal squamous cell carcinoma, Fanconi anemia, Hyperinsulinism, Dermatomyositis, Pancreatic neoplasms, Neurotic disorder, Ovarian cancer, Premature ovarian failure, Pancytopenia, Peripheral vascular disease, Prostate cancer
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163
FA complementation group D2
FA-D2, FA4, FACD, FAD, FAD2, FANCD
Alzheimer disease, Hepatocellular carcinoma, Clear cell renal cell carcinoma, Fanconi anemia, Global developmental delay, Intellectual developmental disorder, Kidney cancer, Pituitary stalk interruption syndrome, Uranostaphyloschisis

164
FANCD2 opposite strand
C3orf24
Alzheimer disease, Cystic kidney disease, Fanconi anemia, Global developmental delay, Intellectual developmental disorder, Kidney disease, Uranostaphyloschisis

165
FA complementation group E
FACE, FAE
Fanconi anemia, Insomnia, Omphalocele exstrophy imperforate anus, Ovarian cancer

166
FA complementation group F
FAF
Fanconi anemia, Parkinson disease

167
FA complementation group G
FAG, XRCC9
Fanconi anemia, Mouth disease, Pituitary stalk interruption syndrome

168
FA complementation group I
KIAA1794
Hepatocellular carcinoma, Fanconi anemia, Immunodeficiency, Insomnia, Mitochondrial disease, Mitochondrial dna depletion syndrome, Schizophrenia, Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis, Hereditary spastic paraplegia

169
FA complementation group L
FAAP43, PHF9, POG
Fanconi anemia, Hypertension, Juvenile idiopathic arthritis, Vacterl association

170
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