Detailed description page of humcfs

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ANTXR1 details
Primary information
gene_nameANTXR1
Humcfs IdHumcfs_782
chromosome_numberchromosome2
nameFRA2E
chrlocation68600001-75000000
cytoband2p13
typeAphidicolin
frequencyCommon
gene_ensembl_idENST00000482235
havana_transcript_idOTTHUMT00000327259
gene_location69075603-69135169
gene_orientation+
exon_idENSE00001817843, ENSE00003504437, ENSE00003579443, ENSE00001360162, ENSE00001360193, ENSE00001190737, ENSE00001898636
exon_number7
gene_descriptionanthrax toxin receptor 1
disease_descriptionSquamous cell carcinoma,Nijmegen Breakage Syndrome,Arteriosclerosis,Fanconi Anemia,Osteosarcoma of bone,Alpha thalassemia-mental retardation syndrome,Cervix carcinoma,ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED,Tooth Crowding,Stomach Carcinoma,Pyothorax-Associated Lymphoma,Chronic Lymphocytic Leukemia,IGA Glomerulonephritis,Infection,Triple Negative Breast Neoplasms,Tumor-Associated Vasculature,Neoplasm Metastasis,Tumor necrosis,HIV Infections,Malignant neoplasm of breast,Breast Carcinoma,Colorectal Cancer,Urothelial Carcinoma,Turcot syndrome (disorder),Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse,melanoma,FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder),Anthrax disease,Carcinoma of lung,Atherosclerosis,Malignant neoplasm of lung,Congenital chromosomal disease,Coronary Artery Disease,Mental Retardation,Dyskeratosis Congenita,alpha-Thalassemia,Myocardial Infarction,Ovarian Carcinoma,Lymphoma,Invasive breast carcinoma,Epithelial o
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID15241441
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