Detailed description page of humcfs

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Humcfs_968 details
Primary information
Humcfs IdHumcfs_968
chromosome_numberchromosome2
nameFRA2K
chrlocation144100001-148700000
cytoband2q22.3
typeFolic acid
frequencyRare
gene_ensembl_idENST00000638043
gene_nameMBD5
havana_transcript_idOTTHUMT00000490541
gene_location148470377-148514333
gene_orientation+
exon_idENSE00003796825, ENSE00001505895, ENSE00001468262, ENSE00003616927, ENSE00003793116, ENSE00003506367, ENSE00003798298]
exon_number7
gene_descriptionmethyl-CpG binding domain protein 5
disease_descriptionSeizures,Shprintzen syndrome,Anxiety Disorders,Fragile X Syndrome,Dysmorphic features,Sleep Disorders,Mental Retardation, Autosomal Dominant 1,Autism Spectrum Disorders,Bipolar Disorder,Neurodevelopmental Disorders,Liver carcinoma,Sleep disturbances,Autistic Disorder,Dyssomnias,Intellectual Disability,Developmental delay (disorder),Epilepsy,Atrial Septal Defects
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