ATFB7
MCID: KCN001
MIFTS: 10

Kcna5-Related Familial Atrial Fibrillation (ATFB7) malady

Categories: Genetic diseases, Rare diseases, Cardiovascular diseases

Aliases & Classifications for Kcna5-Related Familial Atrial Fibrillation

Aliases & Descriptions for Kcna5-Related Familial Atrial Fibrillation:

Name: Kcna5-Related Familial Atrial Fibrillation 24
Atrial Fibrillation, Familial, 7 69
Familial Atrial Fibrillation 7 24
Atfb7 24

Classifications:



Summaries for Kcna5-Related Familial Atrial Fibrillation

MalaCards based summary : Kcna5-Related Familial Atrial Fibrillation, also known as atrial fibrillation, familial, 7, is related to atrial fibrillation, familial, 1 and atrial fibrillation, familial, 7. An important gene associated with Kcna5-Related Familial Atrial Fibrillation is KCNA5 (Potassium Voltage-Gated Channel Subfamily A Member 5).

Related Diseases for Kcna5-Related Familial Atrial Fibrillation

Symptoms & Phenotypes for Kcna5-Related Familial Atrial Fibrillation

Drugs & Therapeutics for Kcna5-Related Familial Atrial Fibrillation

Search Clinical Trials , NIH Clinical Center for Kcna5-Related Familial Atrial Fibrillation

Genetic Tests for Kcna5-Related Familial Atrial Fibrillation

Genetic tests related to Kcna5-Related Familial Atrial Fibrillation:

id Genetic test Affiliating Genes
1 Kcna5-Related Familial Atrial Fibrillation 24 KCNA5

Anatomical Context for Kcna5-Related Familial Atrial Fibrillation

Publications for Kcna5-Related Familial Atrial Fibrillation

Variations for Kcna5-Related Familial Atrial Fibrillation

ClinVar genetic disease variations for Kcna5-Related Familial Atrial Fibrillation:

6
id Gene Variation Type Significance SNP ID Assembly Location
1 KCNA5 NM_002234.3(KCNA5): c.1123G> T (p.Glu375Ter) single nucleotide variant Pathogenic rs121908590 GRCh37 Chromosome 12, 5154436: 5154436
2 KCNA5 NM_002234.3(KCNA5): c.1727C> T (p.Ala576Val) single nucleotide variant Pathogenic rs121908592 GRCh37 Chromosome 12, 5155040: 5155040
3 KCNA5 NM_002234.3(KCNA5): c.1828G> A (p.Glu610Lys) single nucleotide variant Pathogenic rs121908593 GRCh37 Chromosome 12, 5155141: 5155141
4 KCNA5 NM_002234.3(KCNA5): c.143A> G (p.Glu48Gly) single nucleotide variant Pathogenic rs587777336 GRCh37 Chromosome 12, 5153456: 5153456

Expression for Kcna5-Related Familial Atrial Fibrillation

Search GEO for disease gene expression data for Kcna5-Related Familial Atrial Fibrillation.

Pathways for Kcna5-Related Familial Atrial Fibrillation

GO Terms for Kcna5-Related Familial Atrial Fibrillation

Sources for Kcna5-Related Familial Atrial Fibrillation

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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