Detailed description page of humcfs

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Humcfs_5021 details
Primary information
Humcfs IdHumcfs_5021
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000006638
gene_nameTBXA2R
havana_transcript_idOTTHUMT00000453079
gene_location3594552-3600669
gene_orientation-
exon_idENSE00002891889, ENSE00002778126
exon_number2
gene_descriptionthromboxane A2 receptor
disease_descriptionDermatitis, Atopic,Arteriosclerosis,Asthma,Colorectal Cancer,Blood Coagulation Disorders,BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO,Allergic asthma,Bronchial Hyperreactivity,Acute Erythroblastic Leukemia,Neoplasm Metastasis,Coronary Artery Disease,Acute urticaria,Carcinoma of lung,Myeloid Leukemia, Chronic,Malignant neoplasm of lung,Pulmonary Embolism,Myocardial Infarction,Prostatic Neoplasms,Alzheimer's Disease,Cerebrovascular accident,Endotoxemia,Thrombosis,Necrosis,Blood Platelet Disorders,Colorectal Carcinoma,Drug-Induced Liver Injury,Astrocytoma,Asthma, Aspirin-Induced,Epithelial ovarian cancer,Cerebral Infarction,Rhinitis,Childhood asthma,Eczema,Immediate hypersensitivity,Hemorrhagic Disorders
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
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