Detailed description page of humcfs

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Humcfs_4850 details
Primary information
Humcfs IdHumcfs_4850
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000197054
gene_nameZNF763
havana_transcript_idOTTHUMT00000460448
gene_location11965054-11978530
gene_orientation+
exon_idENSE00003566351, ENSE00002735604
exon_number2
gene_descriptionzinc finger protein 763
disease_descriptionFamilial dilated cardiomyopathy,Congenital Abnormality,Neurodegenerative Disorders,Liver carcinoma,Ki-1+ Anaplastic Large Cell Lymphoma,Hepatocarcinogenesis,Merkel cell carcinoma,Kidney Failure, Acute,Xeroderma Pigmentosum,Malignant neoplasm of penis,Neoplasm Metastasis,HIV Infections,Malignant neoplasm of breast,Experimental Autoimmune Encephalomyelitis,Hepatoblastoma,XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E,ovarian neoplasm,Amyotrophic Lateral Sclerosis,Severe Combined Immunodeficiency,Congenital chromosomal disease,Chronic inflammatory disorder,Breast Carcinoma,Virus Diseases,Vitelliform Macular Dystrophy,Diabetes Mellitus, Non-Insulin-Dependent,Lewy Body Disease,Colorectal Neoplasms,Foot Diseases,Autoimmune Diseases,Carcinogenesis,Gastrointestinal Stromal Tumors,leukemia,Systemic Scleroderma,Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site,Leukemia, Myelocytic, Acute,Hepatitis B,Herpes Simplex Infections,Familial primary pul
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank