Detailed description page of humcfs

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Humcfs_2 details
Primary information
Humcfs IdHumcfs_2
chromosome_numberchromosome1
nameFRA1A
chrlocation1-28000000
cytoband1p36
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000157911
gene_namePEX10
havana_transcript_idOTTHUMT00000367454
gene_location2404819-2412571
gene_orientation-
exon_idENSE00001207524, ENSE00001035830, ENSE00003687915, ENSE00001035832, ENSE00003514210, ENSE00001207527
exon_number6
gene_descriptionperoxisomal biogenesis factor 10
disease_descriptionAzoospermia, Nonobstructive,PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER),Zellweger Syndrome,Infantile Refsum Disease (disorder),Azoospermia,PEROXISOME BIOGENESIS DISORDER 6B,Peroxisome biogenesis disorders,Ataxia,Adrenoleukodystrophy, Neonatal,PEROXISOME BIOGENESIS DISORDER 2B
miRNA_location1167878-1167899
miRNA_strand+
miRNA_idMIMAT0001620
miRNA_namehsa-miR-200a-5p
miRNA_derived MI0000737
TechniqueKaryotyping
PMID1322577
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank