Detailed description page of humcfs

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Humcfs_5038 details
Primary information
Humcfs IdHumcfs_5038
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000125726
gene_nameCD70
havana_transcript_idOTTHUMT00000457861
gene_location6590103-6604103
gene_orientation-
exon_idENSE00003784659, ENSE00003138805, ENSE00003135943, ENSE00003178215
exon_number4
gene_descriptionCD70 molecule
disease_descriptionT-Cell Lymphoma,Lupus Erythematosus, Systemic,Diffuse Large B-Cell Lymphoma,Contact Dermatitis,Waldenstrom Macroglobulinemia,Chronic Lymphocytic Leukemia,Nasopharyngeal carcinoma,Chromosome 11p11.2 Deletion Syndrome,Neoplasm Metastasis,Lymphoma, Non-Hodgkin,Epithelioma,Thymoma,Malignant neoplasm of breast,Breast Carcinoma,Lymphoma, Large-Cell, Follicular,Thymoma, type C,melanoma,Lupus Erythematosus, Discoid,Aortic Aneurysm, Thoracic,Precursor Cell Lymphoblastic Leukemia Lymphoma,Renal Cell Carcinoma,Autoimmune Diseases,Acute lymphocytic leukemia,Virus Diseases,PEELING SKIN SYNDROME,Immune thrombocytopenic purpura,Lymphoma,Thymic Carcinoid Tumor,Low Grade Lymphoma (neoplasm),Central neuroblastoma,Hematologic Neoplasms,Rheumatoid Arthritis,leukemia,Lupus Vulgaris,Mycobacterium avium-intracellulare Infection,Leukemia, Myelocytic, Acute,Multiple Myeloma,Systemic Scleroderma,Acute Coronary Syndrome,Anaplastic astrocytoma,Malignant Glioma,Common Variable Immunodeficiency,Thymoma, type B3,Gli
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
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