IGF2

insulin like growth factor 2
OMIM: 147470, Gene2Phenotype

9 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 9 panels
Green IGF2 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.418	review	MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)	Sources Expert Review Green Literature Phenotypes Silver-Russell syndrome 3 MIM#616489
Green IGF2 in Differences of Sex Development Level 2: Dysmorphic and congenital abnormality syndromes Version 0.293	review	MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)	Sources Expert Review Green Literature Phenotypes Silver-Russell syndrome 3 MIM#616489
Green IGF2 in Mendeliome Version 1.1891	review	MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Growth restriction, severe, with distinctive facies, MIM#616489
Green IGF2 in Pierre Robin Sequence Level 2: Dysmorphic and congenital abnormality syndromes Version 0.47	review	MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)	Sources Expert Review Green Literature Phenotypes Silver-Russell syndrome 3 MIM#616489
Red IGF2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	Unknown	Sources Expert Review Red Genetic Health Queensland Phenotypes Growth restriction, severe, with distinctive facies, MIM#616489
Green IGF2 in Clefting disorders Level 3: Dysmorphic disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 0.252	review	MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)	Sources Expert Review Green Literature Phenotypes Silver-Russell syndrome 3 MIM#616489
Green IGF2 in Growth failure Version 1.76	review	MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)	Sources Expert Review Green Genomics England PanelApp Phenotypes Silver-Russell syndrome 3, MIM #616489
Green IGF2 in Imprinting disorders Version 1.3	review	MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)	Sources Expert Review Green Genomics England PanelApp Phenotypes Affected tissue: all Phenotypes resulting from gene over expression: Beckwith-Wiedemann Syndrome (proven effects of dosage alteration rather than gene muation). Phenotype resulting from under expression: Silver-Russell syndrome 3, MIM #616489
Green IGF2 in Fetal anomalies Version 1.255	review	MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)	Sources Expert Review Green Genomics England PanelApp Literature Genetic Health Queensland Phenotypes Growth restriction, severe, with distinctive facies, MIM#616489