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Phenotypes Associated with This Genotype
Genotype
MGI:5499740
Allelic
Composition
Myh9tm7.1Rsad/Myh9tm7.1Rsad
Genetic
Background
involves: BALB/cJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myh9tm7.1Rsad mutation (0 available); any Myh9 mutation (189 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• with neutrophil inclusions in the bone marrow (J:175367)
• with neutrophil inclusions in the bone marrow (J:175367)
• in the bone marrow and spleen (J:175367)
• in the bone marrow and spleen (J:175367)
• contain Myh9 aggregates (J:175367)
• contain Myh9 aggregates (J:175367)
• increased diameter (J:175367)
• increased diameter (J:175367)
• macrothrombocytopenia (J:175367)
• macrothrombocytopenia (J:175367)

homeostasis/metabolism

immune system
• contain Myh9 aggregates (J:175367)
• contain Myh9 aggregates (J:175367)

renal/urinary system
• focal segmental glomerulosclerosis and focal global glomerulosclerosis beginning at 4 months (J:175367)
• focal segmental glomerulosclerosis and focal global glomerulosclerosis beginning at 4 months (J:175367)

vision/eye
• bilateral in some mice (J:175367)
• bilateral in some mice (J:175367)


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/02/2016
MGI 6.02
The Jackson Laboratory