Detailed description page of humcfs

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KCTD7 details
Primary information
gene_nameKCTD7
Humcfs IdHumcfs_2276
chromosome_numberchromosome7
nameFRA7J
chrlocation59900001-77500000
cytoband7q11
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000243335
havana_transcript_idOTTHUMT00000345615
gene_location66628958-66638929
gene_orientation+
exon_idENSE00003810139, ENSE00000976772, ENSE00003807483, ENSE00003811021
exon_number4
gene_descriptionpotassium channel tetramerization domain containing 7
disease_descriptionUnverricht-Lundborg Syndrome,Opsoclonus-Myoclonus Syndrome,Kinsbourne Syndrome,EPILEPSY, PROGRESSIVE MYOCLONIC 3,Neuronal Ceroid-Lipofuscinoses,Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia,Myoclonic Epilepsies, Progressive
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID16236432
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