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Phenotypes Associated with This Genotype
Genotype
MGI:2686835
Allelic
Composition
Phox2bDilp1/Phox2b+
Genetic
Background
involves: BALB/cAnN * C3H/HeN
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Phox2bDilp1 mutation (0 available); any Phox2b mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• abnormal Mendelian ratios suggested that some heterozygous mice die before weaning

vision/eye
• exhibit no pupillary response to light
• pupils fail to constrict in response to the parasympathetic agonist, carbachol

behavior/neurological
• exhibit no pupillary response to light
• pupils fail to constrict in response to the parasympathetic agonist, carbachol

nervous system
• exhibit severe atrophy of the ciliary ganglia at E13.5
• however, the superior cervical ganglion is normal


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
12/17/2024
MGI 6.24
The Jackson Laboratory