Phenotypes associated with this allele

• Allele Symbol: Csnk1g3^{tm1a(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1a, Wellcome Trust Sanger Institute
• Allele ID: MGI:4461713
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Csnk1g3^tm1a(EUCOMM)Wtsi/Csnk1g3^tm1a(EUCOMM)Wtsi	C57BL/6N-Csnk1g3^tm1a(EUCOMM)Wtsi/Wtsi	MGI:5797451

Genotype
MGI:5797451

hm1

• Allelic Composition: Csnk1g3^{tm1a(EUCOMM)Wtsi}/Csnk1g3^{tm1a(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Csnk1g3^{tm1a(EUCOMM)Wtsi}/Wtsi
• Cell Lines: EPD0598_4_H07

Data Sources

IMPC Data for Csnk1g3

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

behavior/neurological

absent pinna reflex ( J:211773 )

IMPC - WTSI

craniofacial

abnormal cranium morphology ( J:211773 )

♂

IMPC - WTSI

growth/size/body

decreased body length ( J:211773 )

♀

IMPC - WTSI

hearing/vestibular/ear

abnormal auditory brainstem response ( J:211773 )

IMPC - WTSI

hematopoietic system

decreased erythrocyte cell number ( J:211773 )

♂

IMPC - WTSI

decreased hematocrit ( J:211773 )

IMPC - WTSI

increased mean corpuscular hemoglobin ( J:211773 )

IMPC - WTSI

homeostasis/metabolism

decreased circulating fructosamine level ( J:211773 )

IMPC - WTSI

increased circulating LDL cholesterol level ( J:211773 )

♂

IMPC - WTSI

decreased circulating alkaline phosphatase level ( J:211773 )

♀

IMPC - WTSI

skeleton

abnormal cranium morphology ( J:211773 )

♂

IMPC - WTSI

decreased bone mineral content ( J:211773 )

♀

IMPC - WTSI