Phenotypes associated with this allele

• Allele Symbol: Cwc22⁺
• Allele Name: wild type
• Allele ID: MGI:3820646
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
ht1	Cwc22^em1(IMPC)Mbp/Cwc22^+	C57BL/6NCrl-Cwc22^em1(IMPC)Mbp/Mmucd	MGI:6262228

Genotype
MGI:6262228

ht1

• Allelic Composition: Cwc22^em1(IMPC)Mbp/Cwc22⁺
• Genetic Background: C57BL/6NCrl-Cwc22^em1(IMPC)Mbp/Mmucd

Data Sources

IMPC Data for Cwc22

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

cardiovascular system

hemorrhage ( J:211773 )

IMPC - UCD

embryo

spina bifida ( J:211773 )

IMPC - UCD

hematopoietic system

abnormal spleen morphology ( J:211773 )

♀

IMPC - UCD

homeostasis/metabolism

increased circulating aspartate transaminase level ( J:211773 )

♀

IMPC - UCD

immune system

abnormal spleen morphology ( J:211773 )

♀

IMPC - UCD

liver/biliary system

abnormal liver morphology ( J:211773 )

IMPC - UCD

nervous system

spina bifida ( J:211773 )

IMPC - UCD

renal/urinary system

cystolithiasis ( J:211773 )

♂

IMPC - UCD

urinary bladder obstruction ( J:211773 )

♂

IMPC - UCD

skeleton

increased bone mineral content ( J:211773 )

♀

IMPC - UCD