Detailed description page of humcfs

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CFB details
Primary information
gene_nameCFB
Humcfs IdHumcfs_1867
chromosome_numberchromosome6
nameFRA6H
chrlocation30400001-46200000
cytoband6p21
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000243649
havana_transcript_idOTTHUMT00000356449
gene_location31948956-31952053
gene_orientation+
exon_idENSE00001957142, ENSE00003546120, ENSE00003642066, ENSE00003619748, ENSE00003521649, ENSE00003605234, ENSE00003578918, ENSE00003565059, ENSE00001905580
exon_number9
gene_descriptioncomplement factor B
disease_descriptionLow Vision,Choroiditis,Malignant neoplasm of stomach,Lupus Erythematosus, Systemic,Macular Degeneration, Age-Related, 1,Choroid Diseases,Macular degeneration,Stomach Carcinoma,Kidney Failure, Acute,Choroidal Neovascularization,Lymphoma, Non-Hodgkin,Hemolytic-Uremic Syndrome,HIV Infections,Peripheral Vascular Diseases,Hepatitis B, Chronic,Coronary heart disease,Psoriasis,Bacterial sepsis,Premature Birth,COMPLEMENT FACTOR B DEFICIENCY,Severe Sepsis,Mental Depression,Meningococcal Infections,Diabetes Mellitus, Insulin-Dependent,Autoimmune Diseases,Acute lymphocytic leukemia,Exudative age-related macular degeneration,Myasthenia Gravis,Spontaneous abortion,Multiple Sclerosis,Geographic Atrophy,Diabetes Mellitus, Non-Insulin-Dependent,Diabetes,Necrotizing Ulcerative Gingivitis,Atypical Hemolytic Uremic Syndrome,Inflammatory Bowel Diseases,Glomerulonephritis,Pancreatic Ductal Adenocarcinoma,Rheumatoid Arthritis,Carcinogenesis,Pyruvate Carboxylase Deficiency Disease,Retinal Diseases,Coinfectio
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueBAC cloned
PMID17290399
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