Detailed description page of humcfs

This page displays user query in tabular form.

Humcfs_2979 details
Primary information
Humcfs IdHumcfs_2979
chromosome_numberchromosome11
nameFRA11B
chrlocation114500001-121200000
cytoband11q23.3
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000137709
gene_namePOU2F3
havana_transcript_idOTTHUMT00000388042
gene_location120305644-120317364
gene_orientation+
exon_idENSE00003700265, ENSE00003695000, ENSE00003696360, ENSE00003789546
exon_number4
gene_descriptionPOU class 2 homeobox 3
disease_descriptionArteriosclerosis,Cervix carcinoma,Deep Vein Thrombosis,Stomach Carcinoma,Vascular Diseases,Malignant neoplasm of stomach,Diabetic Retinopathy,Coronary Artery Disease,Malignant neoplasm of breast,Breast Carcinoma,Coronary heart disease,Coronary Arteriosclerosis,Neonatal alloimmune thrombocytopenia (NAIT),Atherosclerosis,Cardiovascular Diseases,Myelitis,Deep thrombophlebitis,Myocardial Infarction,Arterial thrombosis,Diabetes Mellitus, Non-Insulin-Dependent,Cerebrovascular accident,Optic Neuritis,Alloimmunisation,Giant Cell Arteritis,Restenosis,Acute Coronary Syndrome,aspirin sensitivity,Stroke, Lacunar,Thrombasthenia,Behcet Syndrome,Tobacco Use Disorder,Alloimmune thrombocytopenia,Malignant tumor of cervix,Unspecified visual loss
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID17063465
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank