GRIK2

glutamate ionotropic receptor kainate type subunit 2
OMIM: 138244, Gene2Phenotype

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green GRIK2 in Mendeliome Version 1.3512	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Mental retardation, autosomal recessive, 6 MIM# 611092 Neurodevelopmental disorder with impaired language and ataxia and with or without seizures, MIM# 619580
Green GRIK2 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.267 Component of the following Super Panels: Progressive Neurological Conditions	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Mental retardation, autosomal recessive, 6 MIM# 611092 Neurodevelopmental disorder with impaired language and ataxia and with or without seizures, MIM# 619580
Green GRIK2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health Queensland Phenotypes Mental retardation, autosomal recessive, 6 MIM# 611092 Neurodevelopmental disorder with impaired language and ataxia and with or without seizures, MIM# 619580
Amber GRIK2 in Fetal anomalies Version 1.465	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Genomics England PanelApp Phenotypes Neurodevelopmental disorder with impaired language and ataxia and with or without seizures, MIM# 619580