Phenotypes Associated with This Genotype

Genotype
MGI:6731326

• Allelic Composition: Fgfr1op2^em1(IMPC)Mbp/Fgfr1op2⁺
• Genetic Background: C57BL/6N-Fgfr1op2^em1(IMPC)Mbp/MbpMmucd

Data Sources

IMPC Data for Fgfr1op2

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

embryo

abnormal placenta morphology ( J:211773 )

IMPC - UCD

integument

abnormal skin morphology ( J:211773 )

♀

IMPC - UCD

vision/eye

cataract ( J:211773 )

IMPC - UCD

microphthalmia ( J:211773 )

IMPC - UCD

abnormal retina morphology ( J:211773 )

♂

IMPC - UCD

abnormal vitreous body morphology ( J:211773 )

IMPC - UCD

persistence of hyaloid vascular system ( J:211773 )

IMPC - UCD