EXT2:Ensemblv90

exostosin glycosyltransferase 2
OMIM: 608210, ClinGen, DECIPHER

17 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 17 panels
Green EXT2 in Congenital Disorders of Glycosylation Level 2: Metabolic disorders Version 1.80 Component of the following Super Panels: Metabolic Disorders Superpanel Progressive Neurological Conditions	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Seizures, scoliosis, and macrocephaly syndrome 616682 Exostoses, multiple, type 2 133701 Multiple exostoses type II (Disorders of protein O-glycosylation, O-xylosylglycan synthesis deficiencies)
Green EXT2 in Mendeliome Version 1.3802	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Victorian Clinical Genetics Services Phenotypes Exostoses, multiple, type 2 MIM#133701 Seizures, scoliosis, and macrocephaly syndrome, MIM#616682
Green EXT2 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.309 Component of the following Super Panels: Progressive Neurological Conditions	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Phenotypes Seizures, scoliosis, and macrocephaly syndrome, MIM#616682
Green EXT2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.508	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genetic Health Queensland Phenotypes Seizures, scoliosis, and macrocephaly syndrome, MIM#616682
Green EXT2 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.365	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Illumina TruGenome Clinical Sequencing Services UKGTN Radboud University Medical Center, Nijmegen Expert Review Green NHS GMS Expert list Emory Genetics Laboratory Expert Review Victorian Clinical Genetics Services Phenotypes Exostoses, multiple, type 2 133701
Red EXT2 in CGC_86 Version 0.3	0 reviews	Other	Sources CGC_86 Phenotypes Multiple exostoses type 2
Red EXT2 in NCGC Version 0.3	0 reviews	Other	Sources NCGC Phenotypes Multiple exostoses type 2
Red EXT2 in TCGA_PANCAN_2018 Version 0.3	0 reviews	Other	Sources TCGA_PANCAN_2018 Phenotypes Multiple exostoses type 2
Green EXT2 in Sarcoma Level 2: Cancer susceptibility Version 0.4	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green SA Pathology
Green EXT2 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category A gene Expert Review Green Phenotypes Exostoses, multiple, type 2
Green EXT2 in Fetal anomalies Version 1.482	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Genetic Health Queensland Phenotypes Seizures, scoliosis, and macrocephaly syndrome, MIM#616682 Exostoses, multiple, type 2, MIM# 133701
Red EXT2 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.141	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category A gene Phenotypes Seizures, scoliosis, and macrocephaly syndrome, MIM#616682
Green EXT2 in Congenital Disorders of Glycosylation Level 2: Metabolic disorders Version 2.0	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Seizures, scoliosis, and macrocephaly syndrome 616682 Exostoses, multiple, type 2 133701 Multiple exostoses type II (Disorders of protein O-glycosylation, O-xylosylglycan synthesis deficiencies)
Green EXT2 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Expert Review Green Phenotypes Seizures, scoliosis, and macrocephaly syndrome, MIM#616682
Green EXT2 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 1.0	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Victorian Clinical Genetics Services Expert Review Emory Genetics Laboratory Expert list NHS GMS Expert Review Green Radboud University Medical Center, Nijmegen UKGTN Illumina TruGenome Clinical Sequencing Services Expert Review Green Phenotypes Exostoses, multiple, type 2 133701
Red EXT2 in TCGA_PANCAN_2018 Version 1.0	0 reviews	Other	Sources TCGA_PANCAN_2018 Phenotypes Multiple exostoses type 2
Green EXT2 in Sarcoma Level 2: Cancer susceptibility Version 1.0	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources SA Pathology Expert Review Green