HCN1 Chromosome 5

Hyperpolarization activated cyclic nucleotide gated potassium channel 1
79 variants 79 Health Risk

Upload your DNA to see your personal genotypes for variants in HCN1.

What This Gene Does
The membrane protein encoded by this gene is a hyperpolarization-activated cation channel that contributes to the native pacemaker currents in heart and neurons. The encoded protein can homodimerize or heterodimerize with other pore-forming subunits to form a potassium channel. This channel may act as a receptor for sour tastes. [provided by RefSeq, Oct 2011]
Gene Info
Gene Group
Cyclic nucleotide gated channels
Locus Type
gene with protein product
Location
5p12
Ensembl
ENSG00000164588
Associated Conditions (11)
Developmental and epileptic encephalopathy
24
Early-infantile DEE
Inborn genetic diseases
Generalized epilepsy with febrile seizures plus
type 10
HCN1-related disorder
Epileptic encephalopathy
Febrile seizure (within the age range of 3 months to 6 years)
Seizure
Color vision defect
Key Variants
RS10066808
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 24, Early-infantile DEE
Health Risk
RS1052640717
Conflicting classifications of pathogenicity
Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
Health Risk
RS1156299203
Conflicting classifications of pathogenicity
Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
Health Risk
RS1244303801
Conflicting classifications of pathogenicity
Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
Health Risk
RS1282221978
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, Developmental and epileptic encephalopathy
Health Risk
RS1293979204
Conflicting classifications of pathogenicity
Early-infantile DEE, Early-infantile DEE
Health Risk
RS1335934380
Conflicting classifications of pathogenicity
Early-infantile DEE, Early-infantile DEE
Health Risk
RS1394225411
Conflicting classifications of pathogenicity
Early-infantile DEE, Early-infantile DEE
Health Risk
RS1469192494
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 24, Inborn genetic diseases
Health Risk
RS1485709375
Conflicting classifications of pathogenicity
Inborn genetic diseases, Developmental and epileptic encephalopathy, 24
Health Risk
RS150936707
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 24, Early-infantile DEE
Health Risk
RS1561230533
Conflicting classifications of pathogenicity
Early-infantile DEE, Early-infantile DEE
Health Risk
All Variants (79)
RSID Category Clinical Significance Conditions
RS10066808 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 24, Early-infantile DEE
RS1052640717 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS1156299203 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS1244303801 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS1282221978 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, Developmental and epileptic encephalopathy
RS1293979204 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS1335934380 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS1394225411 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS1469192494 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 24, Inborn genetic diseases
RS1485709375 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Developmental and epileptic encephalopathy, 24
RS150936707 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 24, Early-infantile DEE
RS1561230533 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS1739691061 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 24, Early-infantile DEE
RS1745528455 Health Risk Conflicting classifications of pathogenicity Generalized epilepsy with febrile seizures plus, type 10, Early-infantile DEE
RS180790607 Health Risk Conflicting classifications of pathogenicity Generalized epilepsy with febrile seizures plus, type 10, Early-infantile DEE
RS2112108878 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS2112108977 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS2478181993 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 24, Generalized epilepsy with febrile seizures plus
RS35229491 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS368989823 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS371602396 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS372807250 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS373454105 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS373664268 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS376434225 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, HCN1-related disorder, Early-infantile DEE
RS587777491 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS745452621 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS747975797 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, HCN1-related disorder, Early-infantile DEE
RS748665278 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 24, Inborn genetic diseases
RS754966256 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS756753787 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS759096969 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS760071472 Health Risk Conflicting classifications of pathogenicity Early-infantile DEE, Early-infantile DEE
RS760568557 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS761866949 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS766768359 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS773441535 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS778039525 Health Risk Conflicting classifications of pathogenicity HCN1-related disorder, Early-infantile DEE, HCN1-related disorder
RS780209007 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS794726951 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS886043090 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS975527828 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Early-infantile DEE, Inborn genetic diseases
RS989268235 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Developmental and epileptic encephalopathy, 24
RS1057519548 Health Risk Likely pathogenic Epileptic encephalopathy, Developmental and epileptic encephalopathy, 24
RS1057521989 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 24, Developmental and epileptic encephalopathy
RS1554040120 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 24, Developmental and epileptic encephalopathy
RS2111839421 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 10, Generalized epilepsy with febrile seizures plus
RS2112032137 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 10, Generalized epilepsy with febrile seizures plus
RS2112040618 Health Risk Likely pathogenic
RS2112040690 Health Risk Likely pathogenic Inborn genetic diseases, Early-infantile DEE, Early-infantile DEE
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