JAM2

junctional adhesion molecule 2
OMIM: 606870, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Amber JAM2 in White matter disorders and cerebral calcification - narrow panel Level 2: Neurology Version 7.24 Latest signed off version: v7.0 (30 Apr 2025) Component of the following Super Panels: Childhood onset leukodystrophy	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Basal ganglia calcification, idiopathic, 8, autosomal recessive, OMIM:618824 basal ganglia calcification, idiopathic, 8, autosomal recessive, MONDO:0032938 Tags Q1_26_promote_green
Amber JAM2 in Ataxia and cerebellar anomalies - narrow panel Level 2: Neurology Version 8.72 Latest signed off version: v8.0 (30 Apr 2025) Component of the following Super Panels: Hereditary ataxia and cerebellar anomalies - childhood onset	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Basal ganglia calcification, idiopathic, 8, autosomal recessive, OMIM:618824 basal ganglia calcification, idiopathic, 8, autosomal recessive, MONDO:0032938 Tags Q1_26_promote_green
Green JAM2 in Intracerebral calcification disorders Level 3: Parenchymal brain disorders Level 2: Neurology and neurodevelopmental disorders Version 1.37	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Primary brain calcification
Amber JAM2 in Adult onset neurodegenerative disorder Level 2: Neurology Version 8.21 Latest signed off version: v8.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Basal ganglia calcification, idiopathic, 8, autosomal recessive, OMIM:618824 basal ganglia calcification, idiopathic, 8, autosomal recessive, MONDO:0032938 Fahr syndrome Tags Q1_26_promote_green
Amber JAM2 in Hereditary ataxia with onset in adulthood Level 2: Neurology Version 8.30 Latest signed off version: v8.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Basal ganglia calcification, idiopathic, 8, autosomal recessive, OMIM:618824 basal ganglia calcification, idiopathic, 8, autosomal recessive, MONDO:0032938 Tags Q1_26_promote_green