Detailed description page of humcfs

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CRX details
Primary information
gene_nameCRX
Humcfs IdHumcfs_4141
chromosome_numberchromosome19
nameFRA19A
chrlocation32400001-59128983
cytoband19q13
type5-azacytidine
frequencyCommon
gene_ensembl_idENSG00000105392
havana_transcript_idOTTHUMT00000431053
gene_location47819779-47836314
gene_orientation+
exon_idENSE00002612811, ENSE00000715896, ENSE00002603684
exon_number3
gene_descriptioncone-rod homeobox
disease_descriptionRetinal Dystrophy, Early Onset Severe,Spinocerebellar Ataxia Type 7,Retinitis Pigmentosa,Retinoblastoma,Blind Vision,Neoplasm Metastasis,Night Blindness,Macular dystrophy,Pineal Gland Neoplasm,Hereditary macular dystrophy,LEBER CONGENITAL AMAUROSIS 7,Mental Retardation,pineoblastoma,Developmental delay (disorder),Leber Congenital Amaurosis,Age related macular degeneration,Inflammatory Bowel Diseases,Retinal Degeneration,Congenital keratoglobus,Retinal Diseases,Amelogenesis Imperfecta,Severe visual impairment,Cone dystrophy,Retinal Dystrophies,Optic Atrophy, Hereditary, Leber,Photoreceptor degeneration,Cone-Rod Dystrophy 2,Unspecified visual loss
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID2579891
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