Detailed description page of humcfs

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Humcfs_348 details
Primary information
Humcfs IdHumcfs_348
chromosome_numberchromosome1
nameFRA1F
chrlocation142600001-155000000
cytoband1q21
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000143390
gene_nameRFX5
havana_transcript_idOTTHUMT00000316354
gene_location151344792-151346872
gene_orientation-
exon_idENSE00001717317, ENSE00003647996, ENSE00003624294, ENSE00003532823, ENSE00001045114, ENSE00001724780
exon_number6
gene_descriptionregulatory factor X, 5 (influences HLA class II expression)
disease_descriptionBare Lymphocyte Syndrome, Type II, Complementation Group C,Arteriosclerosis,Bare Lymphocyte Syndrome,Bare Lymphocyte Syndrome, Type II, Complementation Group E,Atherosclerosis,Bare lymphocyte syndrome 2,Congenital chromosomal disease,Major histocompatibility complex class II deficiency,Age related macular degeneration,Colorectal Cancer
miRNA_location153689705-153689793
miRNA_strand-
miRNA_idMI0025919
miRNA_namehsa-mir-8083
miRNA_derived NA
TechniqueBAC clones
PMID27625703
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank