Mouse Genome Informatics
ht
    Myh9tm7.1Rsad/Myh9+
involves: BALB/cJ
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
       
hematopoietic system
• contain Myh9 aggregates
• increased diameter
• macrothrombocytopenia
• in the bone marrow and spleen

homeostasis/metabolism

immune system
• contain Myh9 aggregates

renal/urinary system
• focal segmental glomerulosclerosis and focal global glomerulosclerosis beginning at 4 months

vision/eye
• bilateral in some mice

Mouse Models of Human Disease
OMIM IDRef(s)
Epstein Syndrome 153650 J:175367
Fechtner Syndrome; FTNS 153640 J:175367
May-Hegglin Anomaly; MHA 155100 J:175367
Sebastian Syndrome; SBS 605249 J:175367