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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
exma
exencephaly and severe microphthalmia/anophthalmia
MGI:2180503
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
exma/exma+ FVB/N-exma MGI:2429431
ot2
exma/Y FVB/N-exma MGI:2429428


Genotype
MGI:2429431
ht1
Allelic
Composition
exma/exma+
Genetic
Background
FVB/N-exma
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• patchy coat pigmentation

behavior/neurological

craniofacial
• observed in embryos

skeleton
• observed in embryos

vision/eye
• described as occasional
• observed in 8% of embryos age E9.5- E18.5

nervous system
• observed in 8% of embryos age E9.5- E18.5

integument
• patchy coat pigmentation




Genotype
MGI:2429428
ot2
Allelic
Composition
exma/Y
Genetic
Background
FVB/N-exma
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no transgenic males survive beyond birth

craniofacial
• males were described as showing foreshortened craniofacial features

embryo
• male embryos were typically smaller than normal littermates

growth/size/body
• male embryos were typically smaller than normal littermates

vision/eye
• observed in 83% of embryos age E9.5- E18.5

nervous system
• disorganized forebrain
• observed in 83% of embryos age E9.5- E18.5
• cranial closure defects extended to a level caudal to the external ear indicating that in addition to forebrain and midbrain, the hindbrain neural folds failed to close normally





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory