IGF2

insulin like growth factor 2
OMIM: 147470, ClinGen, DECIPHER

9 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 9 panels
Green IGF2 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.430	1 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 1.6	1 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 1.2302	1 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	1 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 1.63	1 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 0.260	1 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	1 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	1 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 1.313	2 reviews	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