KCNA5

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Web Resources for KCNA5
 ICD-10 search


Genetic Databases
GENE database on KCNA5
Online Mendelian Inheritance in Man (OMIM) on KCNA5
Pharmacogenomics Knowledge Base (pharmGKB) on KCNA5
Catalogue Of Somatic Mutations In Cancer (COSMIC) on KCNA5
Genome information (GenomeNet, KEGG) on KCNA5
SNP database on KCNA5
Protein Knowledgebase (UniProtKB) on KCNA5
Relevant Clinical Literature
Pubmed on KCNA5
RCT with KCNA5
Systematic reviews of KCNA5
KCNA5 in N Eng J Med, Lancet, JAMA, BMJ
KCNA5 in Cochrane Collaboration
TRIP Database on KCNA5
Google Scholar on KCNA5
Bandolier on KCNA5
UK Guidance
SNOMED search
NHS Evidence on KCNA5
Centre for Reviews and Dissemination databases -DARE & NHS EED (evaluates reliability of research)
Nice Guidance on KCNA5
Prodigy Guidance on KCNA5
Other Wikis
Wikipedia on KCNA5 (Less technical, ? quality control)

The KCNA5 gene at 12p13 codes for the 613 amino acid potassium voltage-gated channel subfamily A member 5. It mediates the voltage-dependent potassium channel ion permeability of excitable membranes. Mutations cause familial atrial fibrillation 7 (ATFB7).

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Categories: Clinical genetics | Genes | Channelopathies
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