Phenotypes Associated with This Genotype

Genotype
MGI:3702997

• Allelic Composition: Fgfr1^tm1.1Upir/Fgfr1^tm1.1Upir
• Genetic Background: involves: ICR

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

mortality/aging

embryonic lethality, complete penetrance ( J:78879 )

• phenotype is stated to be similar to that of Fgfr1^tm1Jrt homozygotes; however, no data are presented in J:78879

growth/size/body

abnormal embryonic growth/weight/body size ( J:78879 )

embryo

abnormal developmental patterning ( J:78879 )

abnormal embryonic tissue morphology ( J:78879 )

abnormal neural tube morphology ( J:78879 )

abnormal extraembryonic tissue morphology ( J:78879 )

nervous system

abnormal neural tube morphology ( J:78879 )

abnormal brain morphology ( J:78879 )

craniofacial

abnormal craniofacial morphology ( J:78879 )

cardiovascular system

abnormal heart development ( J:78879 )