Phenotypes associated with this allele

• Allele Symbol: Bex2^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5614697
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Bex2^tm1b(EUCOMM)Hmgu/Bex2^tm1b(EUCOMM)Hmgu	C57BL/6N-Bex2^tm1b(EUCOMM)Hmgu/Ieg	MGI:5756798
ot2	Bex2^tm1b(EUCOMM)Hmgu/Y	C57BL/6N-Bex2^tm1b(EUCOMM)Hmgu/Ieg	MGI:5756797

Genotype
MGI:5756798

hm1

• Allelic Composition: Bex2^{tm1b(EUCOMM)Hmgu}/Bex2^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Bex2^{tm1b(EUCOMM)Hmgu}/Ieg
• Cell Lines: HEPD0727_6_C09

Data Sources

IMPC Data for Bex2

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

behavior/neurological

increased startle reflex ( J:211773 )

♀

IMPC - HMGU

decreased locomotor activity ( J:211773 )

♀

IMPC - HMGU

cardiovascular system

abnormal retina blood vessel morphology ( J:211773 )

♀

IMPC - HMGU

hematopoietic system

decreased red blood cell distribution width ( J:211773 )

♀

IMPC - HMGU

increased leukocyte cell number ( J:211773 )

♀

IMPC - HMGU

immune system

increased leukocyte cell number ( J:211773 )

♀

IMPC - HMGU

integument

abnormal coat/hair pigmentation ( J:211773 )

♀

IMPC - HMGU

nervous system

decreased prepulse inhibition ( J:211773 )

♀

IMPC - HMGU

pigmentation

abnormal coat/hair pigmentation ( J:211773 )

♀

IMPC - HMGU

vision/eye

abnormal retina blood vessel morphology ( J:211773 )

♀

IMPC - HMGU

Genotype
MGI:5756797

ot2

• Allelic Composition: Bex2^{tm1b(EUCOMM)Hmgu}/Y
• Genetic Background: C57BL/6N-Bex2^{tm1b(EUCOMM)Hmgu}/Ieg
• Cell Lines: HEPD0727_6_C09

Data Sources

IMPC Data for Bex2

behavior/neurological

increased startle reflex ( J:211773 )

♂

IMPC - HMGU

decreased locomotor activity ( J:211773 )

♂

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

♂

IMPC - HMGU

abnormal retina morphology ( J:211773 )

♂

IMPC - HMGU