Detailed description page of humcfs

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Humcfs_656 details
Primary information
Humcfs IdHumcfs_656
chromosome_numberchromosome1
nameFRA1L
chrlocation61300001-84900000
cytoband1p31
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000081985
gene_nameIL12RB2
havana_transcript_idOTTHUMT00000487773
gene_location67307873-67395835
gene_orientation+
exon_idENSE00003775461, ENSE00003783434, ENSE00000903840, ENSE00003783155, ENSE00003782631, ENSE00003782588, ENSE00003780343, ENSE00003778869, ENSE00003776645, ENSE00003778639, ENSE00003781545, ENSE000037807
exon_number16
gene_descriptioninterleukin 12 receptor, beta 2
disease_descriptionDermatitis, Atopic,Malignant neoplasm of stomach,Asthma,Leprosy, Lepromatous,Pre-Eclampsia,Plasmacytoma,Periodontal Diseases,Burkitt Lymphoma,Stomach Carcinoma,Dermatitis,Chronic Lymphocytic Leukemia,Adenocarcinoma,Alveolar Bone Loss,Lupus Erythematosus, Systemic,Non-Small Cell Lung Carcinoma,Hyperparathyroidism, Secondary,Rubella,Dermatologic disorders,Fetal Membranes, Premature Rupture,Behcet Syndrome,Cervical Adenocarcinoma,Measles,Diabetes Mellitus, Insulin-Dependent,Mammary Neoplasms,Infection,Biliary cirrhosis,Gram-Negative Bacterial Infections,Tuberculosis,Infection of amniotic sac and membranes, unspecified, unspecified trimester, not applicable or unspecified,Lymphoma,Chronic Periodontitis,Respiratory Syncytial Virus Infections,Anemia,Psoriasis,Systemic arterial pressure,Giant Cell Arteritis,Multiple Myeloma,Premature Birth,Leprosy,Uveomeningoencephalitic Syndrome,Systemic Scleroderma,Periodontitis, Juvenile,Primary biliary cirrhosis,Chorioamnionitis,Blood pressure finding,Gin
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID20198338
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