Detailed description page of humcfs

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Humcfs_1828 details
Primary information
Humcfs IdHumcfs_1828
chromosome_numberchromosome6
nameFRA6H
chrlocation30400001-46200000
cytoband6p21
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000204348
gene_nameDXO
havana_transcript_idOTTHUMT00000076592
gene_location31969813-31972290
gene_orientation-
exon_idENSE00001927710, ENSE00003618801, ENSE00003652569, ENSE00001783226, ENSE00003515583, ENSE00003499064, ENSE00001866894
exon_number7
gene_descriptiondecapping exoribonuclease
disease_descriptionFragile X Syndrome,Lupus Erythematosus, Systemic,Metabolic Syndrome X,Neurodevelopmental Disorders,Sleep disturbances,Autistic Disorder,Chronic Lymphocytic Leukemia,Spinocerebellar Ataxia Type 2,Autism Spectrum Disorders,Smith-Magenis syndrome,Potocki-Lupski syndrome,Hyperphagia,Alzheimer's Disease,Sleep Disorders,Hearing Loss, Mixed Conductive-Sensorineural,Idiopathic Membranous Glomerulonephritis,Obesity,Congenital Heart Defects,Hypercholesterolemia,Intellectual Disability,Schizophrenia,Dyssomnias
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueBAC cloned
PMID17290399
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank