Detailed description page of humcfs

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Humcfs_1206 details
Primary information
Humcfs IdHumcfs_1206
chromosome_numberchromosome3
nameFRA3C
chrlocation182700001-187900000
cytoband3q27
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000214160
gene_nameALG3
havana_transcript_idOTTHUMT00000346035
gene_location184242469-184249520
gene_orientation-
exon_idENSE00001719497, ENSE00003511305, ENSE00003647968, ENSE00003669013, ENSE00003639117, ENSE00003654734, ENSE00003540107, ENSE00003599288, ENSE00001651789
exon_number9
gene_descriptionALG3, alpha-1,3- mannosyltransferase
disease_descriptionCongenital, Hereditary, and Neonatal Diseases and Abnormalities,CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id,Congenital Disorders of Glycosylation
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID8406484
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