NPRL2

NPR2 like, GATOR1 complex subunit
OMIM: 607072, Gene2Phenotype

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green NPRL2 in Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly Level 2: Neurology and neurodevelopmental disorders Version 0.48 Component of the following Super Panels: Malformations of cortical development_Superpanel	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Australian Genomics Health Alliance Brain Malformations Flagship Phenotypes Epilepsy, familial focal, with variable foci 2- MIM#617116
Green NPRL2 in Mendeliome Version 1.3512	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Epilepsy, familial focal, with variable foci 2, MIM# 617116 focal seizures frontal lobe epilepsy nocturnal frontal lobe epilepsy temporal lobe epilepsy focal cortical dysplasia
Green NPRL2 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.267 Component of the following Super Panels: Progressive Neurological Conditions	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Australian Genomics Health Alliance Epilepsy Flagship Phenotypes Epilepsy, familial focal, with variable foci 2 617116 focal seizures frontal lobe epilepsy nocturnal frontal lobe epilepsy temporal lobe epilepsy focal cortical dysplasia
Green NPRL2 in Fetal anomalies Version 1.465	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Epilepsy, familial focal, with variable foci 2 - MIM#617116