Detailed description page of humcfs

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Humcfs_3002 details
Primary information
Humcfs IdHumcfs_3002
chromosome_numberchromosome11
nameFRA11C
chrlocation16200001-21700000
cytoband11p15.1
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000006611
gene_nameUSH1C
havana_transcript_idOTTHUMT00000389149
gene_location17493900-17544400
gene_orientation-
exon_idENSE00002152572, ENSE00003564672, ENSE00003570131, ENSE00003506647, ENSE00003496015, ENSE00003586081, ENSE00003684369, ENSE00000339040, ENSE00000705382, ENSE00000705383, ENSE00000705385, ENSE000007053
exon_number20
gene_descriptionUsher syndrome 1C (autosomal recessive, severe)
disease_descriptionNonsyndromic Deafness,Malignant tumor of colon,Deafness, Autosomal Recessive 18,Retinal Degeneration,Sensorineural Hearing Loss (disorder),Colon Carcinoma,Retinal Diseases,Tobacco Use Disorder,Usher syndrome, type 1C,Usher syndrome, type 1A,Usher Syndrome,Hearing Loss, Mixed Conductive-Sensorineural,Autoimmune enteropathy,Autosomal recessive retinitis pigmentosa,Usher Syndrome, Type I,Adenocarcinoma of large intestine,Congenital deafness,USHER SYNDROME, TYPE IC
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID15771901
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank