PRKD1

protein kinase D1
OMIM: 605435, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green PRKD1 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.418	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Congenital heart defects and ectodermal dysplasia, 617364 Autosomal Recessive Congenital Heart Disease
Green PRKD1 in Mendeliome Version 1.1902	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Congenital heart defects and ectodermal dysplasia, 617364 Congenital heart disease, autosomal recessive
Amber PRKD1 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Genetic Health Queensland Phenotypes Congenital heart defects and ectodermal dysplasia, 617364
Green PRKD1 in Ectodermal Dysplasia Level 2: Dermatological disorders Version 0.86	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Congenital heart defects and ectodermal dysplasia, MIM# 617364
Green PRKD1 in Fetal anomalies Version 1.255	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Genetic Health Queensland Phenotypes Congenital heart defects and ectodermal dysplasia, MIM#617364