Phenotypes associated with this allele

• Allele Symbol: Galk2^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5613648
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Galk2^tm1b(EUCOMM)Hmgu/Galk2^tm1b(EUCOMM)Hmgu	C57BL/6N-Galk2^tm1b(EUCOMM)Hmgu/Ieg	MGI:5797550

Genotype
MGI:5797550

hm1

• Allelic Composition: Galk2^{tm1b(EUCOMM)Hmgu}/Galk2^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Galk2^{tm1b(EUCOMM)Hmgu}/Ieg
• Cell Lines: HEPD0525_3_D02

Data Sources

IMPC Data for Galk2

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

behavior/neurological

increased grip strength ( J:211773 )

♀

IMPC - HMGU

cardiovascular system

cardiovascular system phenotype ( J:211773 )

♀

IMPC - HMGU

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

homeostasis/metabolism

increased circulating bilirubin level ( J:211773 )

♂

IMPC - HMGU

increased circulating alkaline phosphatase level ( J:211773 )

IMPC - HMGU

limbs/digits/tail

abnormal digit morphology ( J:211773 )

♂

IMPC - HMGU

renal/urinary system

abnormal kidney morphology ( J:211773 )

♂

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

IMPC - HMGU

cataract ( 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

abnormal vitreous body morphology ( J:211773 )

IMPC - HMGU

persistence of hyaloid vascular system ( J:211773 )

IMPC - HMGU