ASPN

asporin
OMIM: 608135, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red ASPN in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • {Lumbar disc degeneration} MIM#603932
  • {Osteoarthritis susceptibility 3} MIM#607850