Detailed description page of humcfs

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SSB details
Primary information
gene_nameSSB
Humcfs IdHumcfs_827
chromosome_numberchromosome2
nameFRA2G
chrlocation169700001-183000000
cytoband2p31
typeAphidicolin
frequencyCommon
gene_ensembl_idENST00000409333
havana_transcript_idOTTHUMT00000328175
gene_location169799279-169812064
gene_orientation+
exon_idENSE00001579221, ENSE00003510639, ENSE00003620133, ENSE00002471090, ENSE00002496741, ENSE00003787270, ENSE00003606885, ENSE00003607377, ENSE00003578824, ENSE00003562426, ENSE00000782045, ENSE000015886
exon_number12
gene_descriptionSjogren syndrome antigen B (autoantigen La)
disease_descriptionRaynaud Disease,Bronchiectasis,Lupus Erythematosus, Systemic,Gastric ulcer,Sjogren's Syndrome,Chromosome 11p11.2 Deletion Syndrome,Neutropenia,Graves Disease,Dermatologic disorders,Arthropathy,Lupus Erythematosus, Discoid,Sialadenitis,Arthritis,Autoimmune Diseases,PEELING SKIN SYNDROME,Dengue Fever,Leukopenia,Thyroiditis,Primary Sj_gren's syndrome,Mucosa-Associated Lymphoid Tissue Lymphoma,Rheumatoid Arthritis,Kidney Diseases,Lupus Vulgaris,Pyothorax-Associated Lymphoma,Lung diseases,Systemic Scleroderma,Hepatitis B,Hepatitis C,Primary biliary cirrhosis,Neonatal Systemic lupus erythematosus,Non-Neoplastic Disorder,Congenital heart block,Lupus Erythematosus,Ataxia Telangiectasia
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID12620385
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