HMGA2

high mobility group AT-hook 2
OMIM: 600698, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green HMGA2 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Silver-Russel syndrome, MIM#618908
Tags
  • SV/CNV

Green HMGA2 in Incidentalome_PREGEN_DRAFT


Version 0.43

review Unknown
Sources
  • NSW Health Pathology
  • Expert Review Green

Green HMGA2 in Growth failure


Version 1.76

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Silver-Russell syndrome 5, MIM# 618908
  • MONDO:0020795

Green HMGA2 in Fetal anomalies


Version 1.255

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Silver-Russell syndrome 5, OMIM:618908
  • Silver-Russell syndrome 5, MONDO:0020795
Tags
  • SV/CNV