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  1. Genes and Genomic Entities
  2. CSRP3

CSRP3

cysteine and glycine rich protein 3
OMIM: 600824, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Red CSRP3 in Dilated Cardiomyopathy


Level 2: Cardiovascular disorders
Version 1.48

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Cardiomyopathy_Adult_SuperPanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Cardiomyopathy, dilated, 1M MIM#607482
    Tags
    • disputed

    Green CSRP3 in Hypertrophic cardiomyopathy_HCM


    Level 2: Cardiovascular disorders
    Version 1.10

    Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Cardiomyopathy_Adult_SuperPanel

    		•  2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Cardiomyopathy, hypertrophic, 12, MIM# 612124

    Green CSRP3 in Mendeliome


    Version 1.3512

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • hypertrophic cardiomyopathy12 MIM#612124
    • dilated cardiomyopathy 1M MIM#607482

    Green CSRP3 in Cardiomyopathy_Paediatric


    Level 2: Cardiovascular disorders
    Version 0.207

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • South West GLH
    • NHS GMS
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Cardiomyopathy, dilated, 1M
    • Cardiomyopathy, familial hypertrophic, 12

    Red CSRP3 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    		0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    • BabySeq Category B gene
    Phenotypes
    • Cardiomyopathy, familial hypertrophic, 12
    • Cardiomyopathy, dilated, 1M

    Red CSRP3 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    		0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • BabySeq Category C gene
    • BabySeq Category B gene
    • Expert Review Red
    Phenotypes
    • Cardiomyopathy, dilated, 1M
    • Cardiomyopathy, familial hypertrophic, 12

    Green CSRP3 in Transplant Co-Morbidity


    Level 2: Screening
    Version 0.20

    		0 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Cardiomyopathy, hypertrophic, 12, MIM# 612124