Detailed description page of humcfs

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PPARGC1A details
Primary information
gene_namePPARGC1A
Humcfs IdHumcfs_1395
chromosome_numberchromosome4
nameFRA4D
chrlocation11300001-35800000
cytoband4p15
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000109819
havana_transcript_idOTTHUMT00000360006
gene_location23882679-23890035
gene_orientation-
exon_idENSE00002074290, ENSE00002051147
exon_number2
gene_descriptionperoxisome proliferator-activated receptor gamma, coactivator 1 alpha
disease_descriptionFasting Hypoglycemia,Weight Loss Adverse Event,Macular degeneration,Carotid Atherosclerosis,Fetal Growth Retardation,Amyotrophic Lateral Sclerosis,Overweight,Cardiovascular Diseases,Gestational Diabetes,Idiopathic pulmonary arterial hypertension,Hodgkin Disease,Myocardial Infarction,Epithelial ovarian cancer,Metabolic Syndrome X,Malignant tumor of colon,Nephrotic Syndrome,Multiple Myeloma,Neurodegenerative Disorders,Diabetes Mellitus,Obesity,Kidney Failure, Chronic,Blood pressure finding,Cholesterol gallstones,Sepsis,Muscular Dystrophy, Animal,Hypothyroidism,Age related macular degeneration,Abdominal obesity metabolic syndrome,Takotsubo Cardiomyopathy,Colorectal Cancer,Huntington Disease,Congenital Hypothyroidism,Prostate carcinoma,Right Ventricular Hypertrophy,Sciatic Neuropathy,Cholecystolithiasis,Trichothiodystrophy Syndromes,Diabetic Retinopathy,Malignant neoplasm of breast,Ischemia,Breast Carcinoma,Disorder of eye,Friedreich Ataxia,Hypertriglyceridemia,Chagas Disease,Bowen's Disea
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID17567780
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