Phenotypes associated with this allele

• Allele Symbol: Me2^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5692786
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Me2^tm1b(EUCOMM)Hmgu/Me2^tm1b(EUCOMM)Hmgu	C57BL/6N-Me2^tm1b(EUCOMM)Hmgu/Ieg	MGI:6262858

Genotype
MGI:6262858

hm1

• Allelic Composition: Me2^{tm1b(EUCOMM)Hmgu}/Me2^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Me2^{tm1b(EUCOMM)Hmgu}/Ieg
• Cell Lines: HEPD0528_2_C05

Data Sources

IMPC Data for Me2

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

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

IMPC - HMGU

endocrine/exocrine glands

abnormal seminal vesicle morphology ( J:211773 )

♂

IMPC - HMGU

hematopoietic system

decreased mean corpuscular volume ( J:211773 )

IMPC - HMGU

homeostasis/metabolism

increased circulating bilirubin level ( J:211773 )

IMPC - HMGU

decreased blood urea nitrogen level ( J:211773 )

♀

IMPC - HMGU

increased circulating chloride level ( J:211773 )

IMPC - HMGU

reproductive system

abnormal seminal vesicle morphology ( J:211773 )

♂

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

♀

IMPC - HMGU

cataract ( J:211773 )

♀

IMPC - HMGU

persistence of hyaloid vascular system ( J:211773 )

♀

IMPC - HMGU

abnormal retina morphology ( J:211773 )

♂

IMPC - HMGU

abnormal retina vasculature morphology ( J:211773 )

IMPC - HMGU