Phenotypes associated with this allele

• Allele Symbol: Pkig^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5636975
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Pkig^tm1b(EUCOMM)Hmgu/Pkig^tm1b(EUCOMM)Hmgu	C57BL/6N-Pkig^tm1b(EUCOMM)Hmgu/Ieg	MGI:6263173

Genotype
MGI:6263173

hm1

• Allelic Composition: Pkig^{tm1b(EUCOMM)Hmgu}/Pkig^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Pkig^{tm1b(EUCOMM)Hmgu}/Ieg
• Cell Lines: HEPD0738_3_C12

Data Sources

IMPC Data for Pkig

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

behavior/neurological

increased startle reflex ( J:211773 )

♀

IMPC - HMGU

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

♂

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

IMPC - HMGU

homeostasis/metabolism

increased blood urea nitrogen level ( J:211773 )

♀

IMPC - HMGU

increased circulating alkaline phosphatase level ( J:211773 )

IMPC - HMGU

increased circulating aspartate transaminase level ( J:211773 )

♂

IMPC - HMGU

vision/eye

irregularly shaped pupil ( J:211773 )

♀

IMPC - HMGU

abnormal lens morphology ( 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

decreased total retina thickness ( J:211773 )

♀

IMPC - HMGU