Phenotypes associated with this allele

• Allele Symbol: Wnt10b^{tm1e.1(KOMP)Wtsi}
• Allele Name: targeted mutation 1e.1, Wellcome Trust Sanger Institute
• Allele ID: MGI:5582422
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Wnt10b^tm1e.1(KOMP)Wtsi/Wnt10b^tm1e.1(KOMP)Wtsi	C57BL/6N-Wnt10b^tm1e.1(KOMP)Wtsi/Ucd	MGI:5797914

Genotype
MGI:5797914

hm1

• Allelic Composition: Wnt10b^{tm1e.1(KOMP)Wtsi}/Wnt10b^{tm1e.1(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Wnt10b^{tm1e.1(KOMP)Wtsi}/Ucd
• Cell Lines: EPD0314_2_A09

Data Sources

IMPC Data for Wnt10b

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

digestive/alimentary system

abnormal cecum morphology ( J:211773 )

IMPC - UCD

nervous system

abnormal brain morphology ( J:211773 )

♂

IMPC - UCD

hydrocephaly ( J:211773 )

♂

IMPC - UCD

skeleton

decreased bone mineral content ( J:211773 )

IMPC - UCD

decreased bone mineral density ( J:211773 )

IMPC - UCD