Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "C"
1741 to 1750 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1741
Cytochrome P450 family 1 subfamily B member 1
ASGD6, CP1B, CYPIB1, GLC3A, P4501B1
Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Basal cell carcinoma, Breast neoplasms, Squamous cell carcinoma, Cardiomegaly, Asthma, Colorectal neoplasms, Congenital glaucoma, Congenital ocular coloboma, Contact dermatitis, Coronary artery disease, Melanoma, Glaucoma, Fatty liver
View all (16 more)

1742
Cytochrome P450 family 20 subfamily A member 1
CYP-M
Attention deficit hyperactivity disorder, Insomnia, Myocardial infarction, Osteoarthritis, Respiratory system disease

1743
Cytochrome P450 family 21 subfamily A member 2
CA21H, CAH1, CPS1, CYP21, CYP21B, P450c21B
Atrial fibrillation, Autism, Congenital adrenal hyperplasia due to 21-hydroxylase deficiency, Congenital adrenal hyperplasia, Coronary artery disease, Ehlers-danlos syndrome, Hyperandrogenism, Major depressive disorder, Psoriasis, Systemic lupus erythematosus, Diabetes mellitus type 2, Age-related macular degeneration

1744
Cytochrome P450 family 24 subfamily A member 1
CP24, CYP24, HCAI, HCINF1, P450-CC24
Eczema, Attention deficit hyperactivity disorder, Autism, Bladder calculus, Breast neoplasms, Kidney and ureter calculus, Ulcerative colitis, Colorectal cancer, Diabetic neuropathy, Hypercalcemia, Idiopathic infantile hypercalcemia, Hypercalciuria, Kidney failure, Lung neoplasms, Multiple sclerosis
View all (5 more)

1745
Cytochrome P450 family 26 subfamily A member 1
CP26, CYP26, P450RAI, P450RAI1
Barrett esophagus, Colonic neoplasms, Endometriosis, Esophageal neoplasms, Hyperlipidemia, Liver cirrhosis, Metabolic syndrome

1746
Cytochrome P450 family 26 subfamily B member 1
CYP26A2, P450RAI-2, P450RAI2, RHFCA
Autism, Colorectal adenoma, Craniosynostosis, Desbuquois syndrome, Esophageal squamous cell carcinoma, Mouth disease, Obesity, Osteoarthritis, Psoriasis, Schizophrenia

1747
Cytochrome P450 family 26 subfamily C member 1
FFDD4
Focal facial dermal dysplasia

1748
Cytochrome P450 family 27 subfamily A member 1
CP27, CTX, CYP27
Atherosclerosis, Autism, Bone disease, Cerebrotendinous xanthomatosis, Cholestanol storage disease, Cholelithiasis, Intellectual developmental disorder, Liver cirrhosis, Metabolic bone disorder, Xanthomatosis

1749
Cytochrome P450 family 27 subfamily B member 1
CP2B, CYP1, CYP1alpha, CYP27B, P450c1, PDDR, VDD1, VDDR, VDDRI, VDR
Autism, Desbuquois syndrome, Diabetes mellitus type 1, Hepatitis b, Hypercalcemia, Hypocalcemic vitamin d-dependent rickets, Polymyositis, Multiple sclerosis, Obesity, Rickets, Vitamin d dependent rickets

1750
Cytochrome P450 family 27 subfamily C member 1
-
Autism, Stroke, Upper aerodigestive tract neoplasm