Detailed description page of humcfs

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Humcfs_4962 details
Primary information
Humcfs IdHumcfs_4962
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000178951
gene_nameZBTB7A
havana_transcript_idOTTHUMT00000457622
gene_location4047742-4065732
gene_orientation-
exon_idENSE00003106223, ENSE00001422884, ENSE00003005251
exon_number3
gene_descriptionzinc finger and BTB domain containing 7A
disease_descriptionSquamous cell carcinoma,Thymoma,Fanconi Anemia,Cervix carcinoma,Prostate carcinoma,Chronic Lymphocytic Leukemia,Pituitary Diseases,Neoplasm Metastasis,HIV Infections,Lung Neoplasms,Breast Carcinoma,Precocious Puberty,Malignant neoplasm of prostate,Carcinoma of bladder,Malignant neoplasm of breast,Precursor Cell Lymphoblastic Leukemia Lymphoma,Malignant neoplasm of lung,Developmental Disabilities,Acute lymphocytic leukemia,Lymphoma,Solid tumour,Rheumatoid Arthritis,Carcinogenesis,Prostatic Neoplasms,leukemia,Monosomy,Colorectal Carcinoma,FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder),Chronic arthritis,Cryptogenic sexual precocity,Benign Prostatic Hyperplasia,bone destruction,Non-Small Cell Lung Carcinoma,Chondrosarcoma,Arthritis, Adjuvant-Induced,Carcinoma of lung,Malignant tumor of cervix,Malignant neoplasm of urinary bladder
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
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