Phenotypes associated with this allele

• Allele Symbol: Bnip2^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5636917
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Bnip2^tm1b(EUCOMM)Wtsi/Bnip2^tm1b(EUCOMM)Wtsi	C57BL/6N-Bnip2^tm1b(EUCOMM)Wtsi/Wtsi	MGI:5756805

Genotype
MGI:5756805

hm1

• Allelic Composition: Bnip2^{tm1b(EUCOMM)Wtsi}/Bnip2^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Bnip2^{tm1b(EUCOMM)Wtsi}/Wtsi
• Cell Lines: EPD0431_5_B07

Data Sources

IMPC Data for Bnip2

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

behavior/neurological

increased grip strength ( J:211773 )

♀

IMPC - WTSI

craniofacial

abnormal cranium morphology ( J:211773 )

IMPC - WTSI

abnormal incisor color ( J:211773 )

IMPC - WTSI

growth/size/body

abnormal incisor color ( J:211773 )

IMPC - WTSI

increased lean body mass ( J:211773 )

IMPC - WTSI

hematopoietic system

decreased erythrocyte cell number ( J:211773 )

IMPC - WTSI

increased mean corpuscular hemoglobin ( J:211773 )

♀

IMPC - WTSI

homeostasis/metabolism

increased circulating alkaline phosphatase level ( J:211773 )

♀

IMPC - WTSI

limbs/digits/tail

abnormal femur morphology ( J:211773 )

♂

IMPC - WTSI

abnormal tibia morphology ( J:211773 )

♂

IMPC - WTSI

skeleton

abnormal cranium morphology ( J:211773 )

IMPC - WTSI

abnormal incisor color ( J:211773 )

IMPC - WTSI

abnormal femur morphology ( J:211773 )

♂

IMPC - WTSI

abnormal tibia morphology ( J:211773 )

♂

IMPC - WTSI