Detailed description page of humcfs

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Humcfs_2551 details
Primary information
Humcfs IdHumcfs_2551
chromosome_numberchromosome10
nameFRA10A
chrlocation97000000-1089500001
cytoband10q23.3
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000148737
gene_nameTCF7L2
havana_transcript_idOTTHUMT00000050418
gene_location113152414-113165961
gene_orientation+
exon_idENSE00001956336, ENSE00003620069, ENSE00001938788
exon_number3
gene_descriptiontranscription factor 7-like 2 (T-cell specific, HMG-box)
disease_descriptionWeight Loss Adverse Event,Intestinal Polyposis,Intestinal Cancer,Pregnancy in Diabetics,Congenital diaphragmatic hernia,Nonorganic psychosis,Liver and Intrahepatic Biliary Tract Carcinoma,Calcinosis,HIV Infections,CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3,Mammary Neoplasms,Coronary heart disease,High Grade Intraepithelial Neoplasia,Chronic Kidney Insufficiency,Overweight,Cardiovascular Diseases,Gestational Diabetes,Endometrial Carcinoma,Angelman Syndrome,Encephalopathies,Crohn Disease,Malignant tumor of colon,Diabetes, Autoimmune,Autonomic neuropathy,Fetal Diseases,Prostatic Neoplasms,Multiple malignancy,CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2,Pancreatic carcinoma,Diabetes Mellitus,Obesity,Mental disorders,Intestinal Polyps,Hepatitis, Alcoholic,Brain Neoplasms,Astrocytoma,Intellectual Disability,Tobacco Use Disorder,Colonic Neoplasms,Ileal Diseases,Lymphohistiocytosis, Hemophagocytic,metabolic disturbance,Seizures,Colorectal Cancer,Prostate carcinoma,Neurodevelopmental Disorders,Malignan
miRNA_location101601427-101601448
miRNA_strand-
miRNA_idMIMAT00150321
miRNA_namehsa-miR-3158-3p
miRNA_derived MI0014187
TechniqueKaryotyping
PMID3879149
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