Phenotypes associated with this allele

• Allele Symbol: Msh5^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5629311
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Msh5^tm1b(EUCOMM)Wtsi/Msh5^tm1b(EUCOMM)Wtsi	C57BL/6N-Msh5^tm1b(EUCOMM)Wtsi/Ieg	MGI:6262935

Genotype
MGI:6262935

hm1

• Allelic Composition: Msh5^{tm1b(EUCOMM)Wtsi}/Msh5^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Msh5^{tm1b(EUCOMM)Wtsi}/Ieg
• Cell Lines: EPD0638_1_B02

Data Sources

IMPC Data for Msh5

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

behavior/neurological

increased startle reflex ( J:211773 )

IMPC - HMGU

hematopoietic system

increased leukocyte cell number ( J:211773 )

♀

IMPC - HMGU

homeostasis/metabolism

increased circulating unsaturated transferrin level ( J:211773 )

IMPC - HMGU

immune system

increased leukocyte cell number ( J:211773 )

♀

IMPC - HMGU

skeleton

decreased bone mineral density ( J:211773 )

♀

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

♀

IMPC - HMGU