Phenotypes associated with this allele

• Allele Symbol: Foxd3^tm1.1Lby
• Allele Name: targeted mutation 1.1, Patricia A Labosky
• Allele ID: MGI:2388720
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Foxd3^tm1.1Lby/Foxd3^tm1.1Lby	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * CD-1)	MGI:3662916

Genotype
MGI:3662916

hm1

• Allelic Composition: Foxd3^tm1.1Lby/Foxd3^tm1.1Lby
• Genetic Background: either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * CD-1)

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

mortality/aging

prenatal lethality, complete penetrance ( J:79491 )

• phenotype is stated to be the same as in Foxd3^tm1Lby however, no data is shown in J:79491

embryo

abnormal developmental patterning ( J:79491 )

failure to gastrulate ( J:79491 )

abnormal proximal-distal axis patterning ( J:79491 )

abnormal embryonic epiblast morphology ( J:79491 )

failure of primitive streak formation ( J:79491 )

abnormal extraembryonic endoderm formation ( J:79491 )

cellular

abnormal cell proliferation ( J:79491 )