Detailed description page of humcfs

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CYP21A2 details
Primary information
gene_nameCYP21A2
Humcfs IdHumcfs_1845
chromosome_numberchromosome6
nameFRA6H
chrlocation30400001-46200000
cytoband6p21
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000231852
havana_transcript_idOTTHUMT00000356950
gene_location32038415-32039606
gene_orientation+
exon_idENSE00003588711, ENSE00003548514, ENSE00003462628, ENSE00003643642, ENSE00001956762
exon_number5
gene_descriptioncytochrome P450, family 21, subfamily A, polypeptide 2
disease_descriptionLupus Erythematosus, Systemic,Hyperandrogenism,Urea Cycle Disorders, Inborn,Malignant neoplasm of liver,Virilism,Mineralocorticoid deficiency,Precocious pubarche,Immunoglobulin A deficiency (disorder),Autistic Disorder,Liver and Intrahepatic Biliary Tract Carcinoma,Chronic Lymphocytic Leukemia,Salt-losing congenital adrenal hyperplasia,Acne Vulgaris,Exanthema,Lymphoma, Non-Hodgkin,Addison's disease due to autoimmunity,Adrenal gland hypofunction,Wasting Syndrome,Tumors of Adrenal Cortex,Adrenal hyperplasia,Mild steroid 21-hydroxylase deficiency,11-Beta-hydroxylase deficiency,Precocious Puberty,Polycystic Ovary Syndrome,Premature adrenarche,Spots on skin,21-hydroxylase deficiency,Necrotizing Enterocolitis,Adrenal cortical hypofunction,Addison Disease,Adenoma,Autoimmune Diseases,Cystic Fibrosis,Mental Retardation,Hypoaldosteronism,Spontaneous abortion,Infection by Cryptococcus neoformans,Chronic active hepatitis,Late-onset congenital adrenal hyperplasia,Opportunistic Infections,Deficiency
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueBAC cloned
PMID17290399
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank