SIDT2:Ensemblv90

SID1 transmembrane family member 2
OMIM: 617551, ClinGen, DECIPHER

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Amber SIDT2 in Mendeliome Version 1.3802	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Lysosomal storage disease, MONDO:0002561, SIDT2-related
Amber SIDT2 in Lysosomal Storage Disorder Level 2: Metabolic conditions Version 1.24 Component of the following Super Panels: Metabolic Disorders Superpanel Progressive Neurological Conditions	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Lysosomal storage disease, MONDO:0002561, SIDT2-related
Amber SIDT2 in Regression Level 2: Neurology and neurodevelopmental disorders Version 0.601	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Lysosomal storage disease, MONDO:0002561, SIDT2-related
Amber SIDT2 in Ataxia Level 2: Neurology and neurodevelopmental disorders Version 1.162 Component of the following Super Panels: Ataxia_Superpanel Neuromuscular Superpanel Progressive Neurological Conditions	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Lysosomal storage disease, MONDO:0002561, SIDT2-related
Amber SIDT2 in Lysosomal Storage Disorder Level 2: Metabolic conditions Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Literature Expert Review Amber Phenotypes Lysosomal storage disease, MONDO:0002561, SIDT2-related
Amber SIDT2 in Regression Level 2: Neurology and neurodevelopmental disorders Version 1.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Literature Expert Review Amber Phenotypes Lysosomal storage disease, MONDO:0002561, SIDT2-related