About   Help   FAQ
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 (219 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• with neutrophil inclusions in the bone marrow
• in the bone marrow and spleen
• contain Myh9 aggregates
• increased diameter
• macrothrombocytopenia

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
DO ID OMIM ID(s) Ref(s)
MYH-9 related disease DOID:0060651 OMIM:155100
J:175367


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory