Phenotypes associated with this allele

• Allele Symbol: Csnk1g2^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5613652
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Csnk1g2^tm1b(EUCOMM)Wtsi/Csnk1g2^tm1b(EUCOMM)Wtsi	C57BL/6N-Csnk1g2^tm1b(EUCOMM)Wtsi/Ieg	MGI:6262217

Genotype
MGI:6262217

hm1

• Allelic Composition: Csnk1g2^{tm1b(EUCOMM)Wtsi}/Csnk1g2^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Csnk1g2^{tm1b(EUCOMM)Wtsi}/Ieg
• Cell Lines: EPD0801_6_F07

Data Sources

IMPC Data for Csnk1g2

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

cardiovascular system

abnormal retina vasculature morphology ( J:211773 )

♀

IMPC - HMGU

abnormal retina blood vessel morphology ( J:211773 )

♀

IMPC - HMGU

increased cardiac muscle contractility ( J:211773 )

IMPC - HMGU

increased heart rate variability ( J:211773 )

♂

IMPC - HMGU

hearing/vestibular/ear

abnormal auditory brainstem response ( J:211773 )

IMPC - HMGU

hematopoietic system

increased mean corpuscular volume ( J:211773 )

IMPC - HMGU

homeostasis/metabolism

increased circulating glucose level ( J:211773 )

♂

IMPC - HMGU

increased circulating phosphate level ( J:211773 )

IMPC - HMGU

increased circulating potassium level ( J:211773 )

♀

IMPC - HMGU

increased circulating aspartate transaminase level ( J:211773 )

♀

IMPC - HMGU

muscle

increased cardiac muscle contractility ( J:211773 )

IMPC - HMGU

respiratory system

increased pulmonary respiratory rate ( J:211773 )

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

IMPC - HMGU

persistence of hyaloid vascular system ( 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