Detailed description page of humcfs

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Humcfs_3710 details
Primary information
Humcfs IdHumcfs_3710
chromosome_numberchromosome14
nameFRA14B
chrlocation58100001-67900000
cytoband14q23
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000139988
gene_nameRDH12
havana_transcript_idOTTHUMT00000406918
gene_location67701886-67734452
gene_orientation+
exon_idENSE00002356906, ENSE00002347634, ENSE00001168191, ENSE00000940928, ENSE00000658669, ENSE00001764854, ENSE00000940935, ENSE00000940936, ENSE00002341500
exon_number9
gene_descriptionretinol dehydrogenase 12 (all-trans/9-cis/11-cis)
disease_descriptionLEBER CONGENITAL AMAUROSIS 13,Severe visual impairment,Retinal Degeneration,Retinitis Pigmentosa,Retinal Diseases,Retinal Dystrophies,Optic Atrophy, Hereditary, Leber,Leber Congenital Amaurosis,LEBER CONGENITAL AMAUROSIS 3 (disorder),Autosomal dominant retinitis pigmentosa,Blind Vision,Fundus Albipunctatus,Hyperopia,RETINITIS PIGMENTOSA 53
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID100769
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank