Phenotypes associated with this allele

• Allele Symbol: Paox^{tm1.1(KOMP)Wtsi}
• Allele Name: targeted mutation 1.1, Wellcome Trust Sanger Institute
• Allele ID: MGI:5548591
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Paox^tm1.1(KOMP)Wtsi/Paox^tm1.1(KOMP)Wtsi	C57BL/6N-Paox^tm1.1(KOMP)Wtsi/Ieg	MGI:6263100

Genotype
MGI:6263100

hm1

• Allelic Composition: Paox^{tm1.1(KOMP)Wtsi}/Paox^{tm1.1(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Paox^{tm1.1(KOMP)Wtsi}/Ieg
• Cell Lines: EPD0321_3_E09

Data Sources

IMPC Data for Paox

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

behavior/neurological

hyperactivity ( J:211773 )

♂

IMPC - HMGU

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

♀

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

♀

IMPC - HMGU

increased heart rate variability ( J:211773 )

♂

IMPC - HMGU

hematopoietic system

thrombocytopenia ( J:211773 )

♂

IMPC - HMGU

homeostasis/metabolism

decreased fasting circulating glucose level ( J:211773 )

♀

IMPC - HMGU

increased circulating aspartate transaminase level ( J:211773 )

♂

IMPC - HMGU

vision/eye

abnormal retina vasculature morphology ( J:211773 )

♀

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

♀

IMPC - HMGU