Brugada Syndrome 4 (BRGDA4)

Alias:
Brgda4
Brugada Syndrome, Type 4
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Brugada Syndrome 4, also known as brgda4, is related to retinal cone dystrophy 4 and t cell and nk cell immunodeficiency. An important gene associated with Brugada Syndrome 4 is CACNB2 (Calcium Voltage-Gated Channel Auxiliary Subunit Beta 2), and among its related pathways/superpathways are Activation of cAMP-Dependent PKA and Integrin Pathway. Affiliated tissues include heart and heart-atrium, and related phenotypes are syncope and atrial fibrillation
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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20
161
4

Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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