Detailed description page of humcfs

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FCER2 details
Primary information
gene_nameFCER2
Humcfs IdHumcfs_5063
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000104921
havana_transcript_idOTTHUMT00000461832
gene_location7688776-7702146
gene_orientation-
exon_idENSE00003182652, ENSE00003628227, ENSE00003672754, ENSE00003487649, ENSE00003515231, ENSE00003609356, ENSE00003622475, ENSE00003584257, ENSE00003537804, ENSE00003529945, ENSE00001237098
exon_number11
gene_descriptionFc fragment of IgE, low affinity II, receptor for (CD23)
disease_descriptionHypogammaglobulinemia,Dermatitis, Atopic,Asthma,Hyper-IgM Immunodeficiency Syndrome, Type 1,Nasopharyngeal carcinoma,X-linked agammaglobulinemia,Astler-Coller B1 Rectal Carcinoma,Burkitt Lymphoma,Monocytoid B-cell lymphoma,Chronic Lymphocytic Leukemia,Bronchial Hyperreactivity,Lung Diseases, Interstitial,Allergic asthma,Lymphoma, Non-Hodgkin,Graves Disease,HIV Infections,Parasitic Diseases,Hairy Cell Leukemia,Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse,Food Allergy,Nasal Polyps,Acute urticaria,Arthritis,Diabetes Mellitus, Insulin-Dependent,Malignant neoplasm of lung,Mastocytosis, Systemic,Superinfection,Hypergammaglobulinemia,Trisomy,Hepatitis C, Chronic,Lymphoma,Acquired Immunodeficiency Syndrome,Schistosomiasis,Atopy,Splenic Marginal Zone B-Cell Lymphoma,Wiskott-Aldrich Syndrome,Allergic disposition,secondary acute myeloid leukemia,Rheumatoid Arthritis,leukemia,Multiple Myeloma,Splenic Diffuse Large B-Cell Lymphoma,Marginal Zone B-Cell Lymphoma,Lymphocytosi
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
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