Detailed description page of humcfs

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SPTB details
Primary information
gene_nameSPTB
Humcfs IdHumcfs_3676
chromosome_numberchromosome14
nameFRA14B
chrlocation58100001-67900000
cytoband14q23
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000070182
havana_transcript_idOTTHUMT00000414076
gene_location64746283-64879883
gene_orientation-
exon_idENSE00003487173, ENSE00003615947, ENSE00003496785, ENSE00003615523, ENSE00001364447, ENSE00000658438, ENSE00000867589, ENSE00000392084, ENSE00000902493, ENSE00000902494, ENSE00000867585, ENSE000008675
exon_number36
gene_descriptionspectrin, beta, erythrocytic
disease_descriptionCerebrovascular accident,ELLIPTOCYTOSIS 3,Obesity,SPHEROCYTOSIS, TYPE 1 (disorder),Amyotrophic Lateral Sclerosis,Anemia, hereditary spherocytic hemolytic,Tobacco Use Disorder,Anemia, Neonatal,Malaria, Falciparum,Hereditary pyropoikilocytosis,Myopathy,Anemia, Hemolytic,Uterine Fibroids,Hereditary spherocytosis,Elliptocytosis, Hereditary,Brain Ischemia
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID100769
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