Detailed description page of humcfs

This page displays user query in tabular form.

Humcfs_1256 details
Primary information
Humcfs IdHumcfs_1256
chromosome_numberchromosome3
nameFRA3D
chrlocation148900001-160700000
cytoband3p25
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000163646
gene_nameCLRN1
havana_transcript_idOTTHUMT00000277060
gene_location150926567-150972999
gene_orientation-
exon_idENSE00001342698, ENSE00003573924, ENSE00001230843
exon_number3
gene_descriptionclarin 1
disease_descriptionRetinal Degeneration,Ear Diseases,Retinitis Pigmentosa,RETINITIS PIGMENTOSA 61,Usher Syndrome, Type III,Congenital cataract,Usher Syndrome,Hearing Loss, Mixed Conductive-Sensorineural,Autosomal recessive retinitis pigmentosa,Bilateral cataracts (disorder),Cataract
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID17567780
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank