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Phenotypes Associated with This Genotype
Genotype
MGI:3574274
Allelic
Composition
Cecr2Gt(pGT1)1Hemc/Cecr2Gt(pGT1)1Hemc
Genetic
Background
involves: 129P2/OlaHsd * BALB/c
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cecr2Gt(pGT1)1Hemc mutation (0 available); any Cecr2 mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most homozygous mutants die perinatally, however 7.5% of homozgygotes are found at weaning and these are indistinguishable from wildtype

vision/eye
• some homozygous mutants lacked eyelids

nervous system
• neural tube defect exencephaly was observed at a frequency of 67% in homozygotes

Mouse Models of Human Disease
OMIM ID Ref(s)
Anencephaly 206500 J:96325


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/27/2016
MGI 6.05
The Jackson Laboratory