Detailed description page of humcfs

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Humcfs_2799 details
Primary information
Humcfs IdHumcfs_2799
chromosome_numberchromosome10
nameFRA10D
chrlocation74900000-1070600001
cytoband10q22.1
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000165841
gene_nameCYP2C19
havana_transcript_idOTTHUMT00000049492
gene_location94762681-94776450
gene_orientation+
exon_idENSE00002446586, ENSE00003600653, ENSE00001957849
exon_number3
gene_descriptioncytochrome P450, family 2, subfamily C, polypeptide 19
disease_descriptionLupus Erythematosus, Systemic,Bladder Neoplasm,Cancer of Head and Neck,Helicobacter Infections,T-Cell Lymphoma,Malignant neoplasm of esophagus,Osteochondritis Dissecans,HIV Infections,Mammary Neoplasms,Coronary heart disease,Psoriasis,First myocardial infarction,ovarian neoplasm,Stable angina,Acute Kidney Tubular Necrosis,Pharyngitis,Laryngeal cleft,Cardiovascular Diseases,Gastritis, Atrophic,Coronary Thrombosis,Cirrhosis,Coronary Stenosis,Chronic Kidney Diseases,Myocardial Infarction,Mycoses,Esophageal Neoplasms,Dyspepsia,Rheumatoid Arthritis,Diarrhea,Prostatic Neoplasms,Violence,Thrombosis,Multiple Myeloma,Drug Allergy,Cancer of Digestive System,Biliary Tract Neoplasm,Diabetes Mellitus,Obesity,Mental disorders,Sore Throat,Kidney Failure, Chronic,Digestive System Neoplasms,Myeloid Leukemia,Pleural Neoplasms,Chronic liver disease,Healing ulcer,Heartburn,Seizures,Multiple Chemical Sensitivity,Anxiety Disorders,Congenital adrenal hyperplasia due to 21 hydroxylase deficiency,Stomach Disea
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID16221525
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