MCID: SCK013

Sick Sinus Syndrome 2, Autosomal Dominant malady

Genetic diseases (common) category

Summaries for Sick Sinus Syndrome 2, Autosomal Dominant

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34MalaCards
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MalaCards: Sick Sinus Syndrome 2, Autosomal Dominant An important gene associated with Sick Sinus Syndrome 2, Autosomal Dominant is HCN4 (hyperpolarization activated cyclic nucleotide-gated potassium channel 4).

Aliases & Classifications for Sick Sinus Syndrome 2, Autosomal Dominant

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21GeneTests, 23GTR
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Classifications:

Malacards categories (disease lists): (See all malacards categories)
Global: Genetic diseases (common)


Aliases & Descriptions:

sick sinus syndrome 2, autosomal dominant 21 23


Related Diseases for Sick Sinus Syndrome 2, Autosomal Dominant

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Diseases in the Sick Sinus Syndrome 1, Autosomal Recessive family:

sick sinus syndrome 2, autosomal dominant

Symptoms for Sick Sinus Syndrome 2, Autosomal Dominant

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Drugs & Therapeutics for Sick Sinus Syndrome 2, Autosomal Dominant

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Sources:
6CenterWatch, 43NIH Clinical Center, 7ClinicalTrials
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Approved drugs:

Search CenterWatch for Sick Sinus Syndrome 2, Autosomal Dominant

Drug clinical trials:

Search ClinicalTrials for Sick Sinus Syndrome 2, Autosomal Dominant

Search NIH Clinical Center for Sick Sinus Syndrome 2, Autosomal Dominant

Search CenterWatch for Sick Sinus Syndrome 2, Autosomal Dominant

Genetic Tests for Sick Sinus Syndrome 2, Autosomal Dominant

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21GeneTests, 23GTR
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Genetic tests related to Sick Sinus Syndrome 2, Autosomal Dominant:

id Genetic test Affiliating Genes
1 Sick Sinus Syndrome 2, Autosomal Dominant21 23 HCN4

Anatomical Context for Sick Sinus Syndrome 2, Autosomal Dominant

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Animal Models for Sick Sinus Syndrome 2, Autosomal Dominant or affiliated genes

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Publications for Sick Sinus Syndrome 2, Autosomal Dominant

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Variations for Sick Sinus Syndrome 2, Autosomal Dominant

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1 National Center for Biotechnology Information (Clinvar)
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Clinvar genetic disease variations for Sick Sinus Syndrome 2, Autosomal Dominant:

1
id Gene Name Type Significance SNP ID Assembly Location
1HCN4NM_005477.2(HCN4): c.2016C> A (p.Ser672Arg)single nucleotide variantPathogenicrs104894488GRCh37Chr 15, 73616557: 73616557
2HCN4NM_005477.2(HCN4): c.1657G> A (p.Asp553Asn)single nucleotide variantPathogenicrs104894485GRCh37Chr 15, 73617719: 73617719
3HCN4NM_005477.2(HCN4): c.1438G> C (p.Gly480Arg)single nucleotide variantPathogenicrs121908411GRCh37Chr 15, 73622066: 73622066

Expression for genes affiliated with Sick Sinus Syndrome 2, Autosomal Dominant

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2BioGPS, 16Gene Expression Omnibus DataSets
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Expression patterns in normal tissues for genes affiliated with Sick Sinus Syndrome 2, Autosomal Dominant

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Pathways for genes affiliated with Sick Sinus Syndrome 2, Autosomal Dominant

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Compounds for genes affiliated with Sick Sinus Syndrome 2, Autosomal Dominant

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GO Terms for genes affiliated with Sick Sinus Syndrome 2, Autosomal Dominant

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Products for genes affiliated with Sick Sinus Syndrome 2, Autosomal Dominant

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  • Antibodies
  • Proteins
  • Lysates
  • Antibodies

Sources for Sick Sinus Syndrome 2, Autosomal Dominant

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4CDC
14ExPASy
15FMA
23GTR
24HGMD
25HMDB
26ICD10
27ICD10 via Orphanet
28ICD9CM
30IUPHAR
31KEGG
36MeSH
37MESH via Orphanet
38MGI
41NCIt
42NDF-RT
45NINDS
46Novoseek
48OMIM
49OMIM via Orphanet
53PubMed
54QIAGEN
60SNOMED-CT via Orphanet
63UMLS
64UMLS via Orphanet