Phenotypes Associated with This Genotype

Genotype
MGI:5499738

• Allelic Composition: Myh9^tm7.1Rsad/Myh9⁺
• Genetic Background: involves: BALB/cJ

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

hematopoietic system

increased megakaryocyte cell number ( J:175367 )

• in the bone marrow and spleen

abnormal neutrophil morphology ( J:175367 )

• contain Myh9 aggregates

abnormal platelet morphology ( J:175367 )

• increased diameter

thrombocytopenia ( J:175367 )

• macrothrombocytopenia

homeostasis/metabolism

increased bleeding time ( J:175367 )

albuminuria ( J:175367 )

immune system

abnormal neutrophil morphology ( J:175367 )

• contain Myh9 aggregates

renal/urinary system

albuminuria ( J:175367 )

glomerulosclerosis ( J:175367 )

• focal segmental glomerulosclerosis and focal global glomerulosclerosis beginning at 4 months

vision/eye

cataract ( J:175367 )

• 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