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Human Disease and Mouse Model Detail
Human Disease

Term: Glanzmann Thrombasthenia; GT
OMIM ID: 273800

Synonyms Bleeding Disorder, Platelet-Type, 2; BDPLT2; Glycoprotein Complex IIb-IIIa, Deficiency of; Gp Iib-Iiia Complex, Deficiency of; Platelet Fibrinogen Receptor, Deficiency of; Platelet Glycoprotein IIb-IIIa Deficiency; Thrombasthenia of Glanzmann and Naegeli
Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
     
Itga2b ITGA2B
Itgb3 ITGB3
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory