TRIM47

tripartite motif containing 47
OMIM: 611041, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red TRIM47 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Genetic cerebral small vessel disease MONDO:0018787

Red TRIM47 in Stroke


Level 2: Neurology and neurodevelopmental disorders
Version 1.16

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Genetic cerebral small vessel disease MONDO:0018787