Phenotypes associated with this allele

• Allele Symbol: Me3^{tm1b(KOMP)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5629317
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Me3^tm1b(KOMP)Wtsi/Me3^tm1b(KOMP)Wtsi	C57BL/6N-Me3^tm1b(KOMP)Wtsi/Ieg	MGI:5797652

Genotype
MGI:5797652

hm1

• Allelic Composition: Me3^{tm1b(KOMP)Wtsi}/Me3^{tm1b(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Me3^{tm1b(KOMP)Wtsi}/Ieg
• Cell Lines: EPD0153_4_E12

Data Sources

IMPC Data for Me3

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

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

♂

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

IMPC - HMGU

cataract ( J:211773 )

IMPC - HMGU

abnormal retina morphology ( J:211773 )

♂

IMPC - HMGU

abnormal retina vasculature morphology ( J:211773 )

♂

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

♂

IMPC - HMGU