Detailed description page of humcfs

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Humcfs_3188 details
Primary information
Humcfs IdHumcfs_3188
chromosome_numberchromosome11
nameFRA11H
chrlocation63400001-77100000
cytoband11q13
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000175538
gene_nameKCNE3
havana_transcript_idOTTHUMT00000385536
gene_location74457406-74467549
gene_orientation-
exon_idENSE00002141413, ENSE00001184057, ENSE00002182036, ENSE00002197944
exon_number4
gene_descriptionpotassium channel, voltage gated subfamily E regulatory beta subunit 3
disease_descriptionBrugada Syndrome 6,Hypokalemic periodic paralysis,Syncope,Astigmatism,Atrial Fibrillation,Lone atrial fibrillation,Thyrotoxic periodic paralysis,Paramyotonia Congenita (disorder),Familial Periodic Paralysis,Hyperkalemic periodic paralysis,Hypokalemic periodic paralysis type 1,Long QT Syndrome,Brugada Syndrome (disorder),Neuroleptic Malignant Syndrome,periodic paralysis (finding)
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID23852038
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank