KCNB1 Chromosome 20

Potassium voltage-gated channel subfamily B member 1
145 variants 145 Health Risk

Upload your DNA to see your personal genotypes for variants in KCNB1.

What This Gene Does
Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shab-related subfamily. This member is a delayed rectifier potassium channel and its activity is modulated by some other family members. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Potassium voltage-gated channels|BTB domain containing"
Locus Type
gene with protein product
Location
20q13.13
Ensembl
ENSG00000158445
Associated Conditions (14)
Developmental and epileptic encephalopathy
26
KCNB1-related disorder
Inborn genetic diseases
Epileptic encephalopathy
See cases
Seizure
6 conditions
Intellectual disability
developmental encephalopathy with epilepsy
Myoclonic absence seizure
Epilepsy
Neurodevelopmental delay
Marfanoid habitus and intellectual disability
Key Variants
RS1131691752
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
Health Risk
RS1209493320
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 26, KCNB1-related disorder
Health Risk
RS1256695300
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
Health Risk
RS1276378675
Conflicting classifications of pathogenicity
Inborn genetic diseases, Developmental and epileptic encephalopathy, 26
Health Risk
RS1304300872
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
Health Risk
RS1391326211
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
Health Risk
RS142461221
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
Health Risk
RS1433173706
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 26, Inborn genetic diseases
Health Risk
RS1447311755
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 26, Inborn genetic diseases
Health Risk
RS147498424
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 26, KCNB1-related disorder
Health Risk
RS1569017114
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
Health Risk
RS1569017123
Conflicting classifications of pathogenicity
Epileptic encephalopathy, Developmental and epileptic encephalopathy, 26
Health Risk
All Variants (145)
RSID Category Clinical Significance Conditions
RS896349825 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 26, Inborn genetic diseases
RS936778119 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS947355756 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1057518621 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1057521887 Health Risk Likely pathogenic
RS1057524688 Health Risk Likely pathogenic
RS1060499592 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1060499607 Health Risk Likely pathogenic
RS1064795048 Health Risk Likely pathogenic
RS1131691489 Health Risk Likely pathogenic
RS1191639138 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1555889084 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Seizure
RS1555889090 Health Risk Likely pathogenic Epileptic encephalopathy, Developmental and epileptic encephalopathy, 26
RS1555889103 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1555889108 Health Risk Likely pathogenic Epileptic encephalopathy, Developmental and epileptic encephalopathy, 26
RS1555889127 Health Risk Likely pathogenic 6 conditions, Epileptic encephalopathy, Developmental and epileptic encephalopathy
RS1568658507 Health Risk Likely pathogenic Epileptic encephalopathy, Epileptic encephalopathy
RS1569016820 Health Risk Likely pathogenic Intellectual disability, Intellectual disability
RS1569017025 Health Risk Likely pathogenic Intellectual disability, Intellectual disability
RS1569017160 Health Risk Likely pathogenic Intellectual disability, Intellectual disability, Intellectual disability
RS1601070913 Health Risk Likely pathogenic
RS1601071099 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1601071350 Health Risk Likely pathogenic
RS1601071747 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1601072041 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1984233764 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1984248125 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1984248540 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1984250089 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1984252463 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1984259606 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1984260160 Health Risk Likely pathogenic
RS1984261678 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS1984276555 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS2146812849 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS2146813509 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS2146813611 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS2146813670 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS2146813832 Health Risk Likely pathogenic
RS2146813885 Health Risk Likely pathogenic
RS2146814335 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS2516850088 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS2516851569 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS2516851607 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS2516851908 Health Risk Likely pathogenic KCNB1-related disorder, KCNB1-related disorder
RS2516852481 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Developmental and epileptic encephalopathy
RS918313461 Health Risk Likely pathogenic Inborn genetic diseases, Developmental and epileptic encephalopathy, 26
RS959316981 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 26, Epileptic encephalopathy
RS1179351306 Health Risk Pathogenic Epileptic encephalopathy, Epileptic encephalopathy
RS1555889069 Health Risk Pathogenic
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