MCID: SCK013

Sick Sinus Syndrome 2, Autosomal Dominant malady

Genetic diseases (common) category
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Summaries for Sick Sinus Syndrome 2, Autosomal Dominant

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33MalaCards
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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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20GeneTests, 22GTR
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Classifications:

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Global: Genetic diseases (common)


Aliases & Descriptions:

sick sinus syndrome 2, autosomal dominant 20 22


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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42NIH Clinical Center, 6ClinicalTrials
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Drug clinical trials:

Search ClinicalTrials for Sick Sinus Syndrome 2, Autosomal Dominant

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

Genetic Tests for Sick Sinus Syndrome 2, Autosomal Dominant

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20GeneTests, 22GTR
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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 Dominant20 22 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, 15Gene 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
13ExPASy
14FMA
22GTR
23HGMD
24HMDB
25ICD10
26ICD10 via Orphanet
27ICD9CM
29IUPHAR
30KEGG
35MeSH
36MESH via Orphanet
37MGI
40NCIt
41NDF-RT
44NINDS
45Novoseek
47OMIM
48OMIM via Orphanet
52PubMed
53QIAGEN
59SNOMED-CT via Orphanet
62UMLS
63UMLS via Orphanet