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Phenotypes Associated with This Genotype
Genotype
MGI:3580671
Allelic
Composition
Ift88fxo/Ift88fxo
Genetic
Background
C3.B6J-Ift88fxo
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ift88fxo mutation (1 available); any Ift88 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• development is arrested at E12.5-E13.5

nervous system
• lack of ventral midline groove in the neural plate
• sharp angle to mesencephalic flexure at E9.5-E10.5

limbs/digits/tail
• preaxial polydactyly

embryo
• lack of ventral midline groove in the neural plate


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory