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Phenotypes Associated with This Genotype
Genotype
MGI:2661992
Allelic
Composition
Insl3tm1Par/Insl3+
Genetic
Background
involves: 129/Sv * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Insl3tm1Par mutation (0 available); any Insl3 mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• 75% of neonatal males had partial unilateral cryptorchism
• 25% of neonatal males had partial bilateral cryptorchism
• all adult males had fully descended testes
• 25% of neonatal males had partial bilateral cryptorchism
• 75% of neonatal males had partial unilateral cryptorchism

reproductive system
• 75% of neonatal males had partial unilateral cryptorchism
• 25% of neonatal males had partial bilateral cryptorchism
• all adult males had fully descended testes
• 25% of neonatal males had partial bilateral cryptorchism
• 75% of neonatal males had partial unilateral cryptorchism
• delayed gubernacular regression

skeleton
• delayed gubernacular regression

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cryptorchidism DOID:11383 OMIM:219050
J:55881


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
11/05/2024
MGI 6.24
The Jackson Laboratory