PanelApp (staging)
  1. Genes and Genomic Entities
  2. CORIN

CORIN

corin, serine peptidase
OMIM: 605236, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red CORIN in Hypertrophic cardiomyopathy_HCM


Level 2: Cardiovascular disorders
Version 1.0

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Cardiomyopathy_Adult_SuperPanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • ?Cardiomyopathy, familial hypertrophic, 30, atrial (MIM:620734)

    Red CORIN in Mendeliome


    Version 1.2302

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Preeclampsia/eclampsia 5 MIM#614595
    • Cardiomyopathy, familial hypertrophic, 30, atrial (MIM:620734)

    Red CORIN in Atrial Fibrillation


    Level 2: Cardiovascular disorders
    Version 1.2

    Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Arrhythmia_SuperPanel

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • ?Cardiomyopathy, familial hypertrophic, 30, atrial (MIM:620734)