UBR2

ubiquitin protein ligase E3 component n-recognin 2
OMIM: 609134, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red UBR2 in Primary Ovarian Insufficiency_Premature Ovarian Failure

Level 3: Gonadal and sex development disorders
Level 2: Endocrine disorders
Version 0.328

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Primary ovarian failure