Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4501 to 4510 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4501
FANCD2 opposite strand
C3orf24
Alzheimer disease, Cystic kidney disease, Fanconi anemia, Global developmental delay, Intellectual developmental disorder, Kidney disease, Uranostaphyloschisis

4502
FA complementation group E
FACE, FAE
Fanconi anemia, Insomnia, Omphalocele exstrophy imperforate anus, Ovarian cancer

4503
FA complementation group F
FAF
Fanconi anemia, Parkinson disease

4504
FA complementation group G
FAG, XRCC9
Fanconi anemia, Mouth disease, Pituitary stalk interruption syndrome

4505
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

4506
FA complementation group L
FAAP43, PHF9, POG
Fanconi anemia, Hypertension, Juvenile idiopathic arthritis, Vacterl association

4507
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

4508
Fibronectin type III and ankyrin repeat domains 1
HSD13
Hypertension

4509
Fibroblast activation protein alpha
DPPIV, FAPA, FAPalpha, SIMP
Ankylosing spondylitis, Eczema, Autoimmune disease, Coronary artery disease, Crohn disease, Hypothyroidism, Inflammatory bowel disease, Inflammatory skin disease, Psoriasis, Psoriasis vulgaris, Psoriatic arthritis, Sclerosing cholangitis, Scoliosis, Systemic lupus erythematosus, Diabetes mellitus type 1
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4510
Fatty acyl-CoA reductase 1
CSPSD, MLSTD2, PFCRD, SDR10E1
Spastic paraplegia, Cataract-neurodevelopmental syndrome, Desbuquois syndrome, Peroxisomal fatty acyl-coa reductase 1 disorder