Source: ANIMAL_MODELS

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9321
Gene Symbol: TRIP11
TRIP11
CUI: C0265273
Disease: Achondrogenesis type 1A
Achondrogenesis type 1A
0.910 Biomarker MGD The similarities between the skeletal and cellular phenotypes in these mice and those in patients with achondrogenesis type 1A, a neonatal lethal form of skeletal dysplasia in humans, suggested that achondrogenesis type 1A may be caused by GMAP-210 deficiency. 20089971

2010