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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Slc35g3em1Osb
endonuclease-mediated mutation 1, Research Institute for Microbial Diseases, Osaka University
MGI:8325060
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Slc35g3em1Osb/Slc35g3em1Osb involves: C57BL/6 * DBA/2 MGI:8325061
cx2
Slc35g3em1Osb/Slc35g3em1Osb
Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0
involves: C57BL/6 * DBA/2 MGI:8325063


Genotype
MGI:8325061
hm1
Allelic
Composition
Slc35g3em1Osb/Slc35g3em1Osb
Genetic
Background
involves: C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Slc35g3em1Osb mutation (0 available); any Slc35g3 mutation (20 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• sperm exhibit abnormal head morphology, with sperm heads lacking the hook shape
• males are sterile despite successful copulation as evidenced by the presence of vaginal plugs
• however, testes appear normal and no overt abnormalities of the seminiferous tubules or epididymis are seen
• in IVF with cumulus-intact oocytes, no oocytes are fertilized with mutant spermatozoa
• ZP-free oocytes show lower number of mutant sperm fusing with the wild-type oocyte
• oolemma fusion and fertilization are improved with 10 times higher mutant sperm concentration but are still decreased compared to the lower concentrations of sperm from controls
• IVF with cumulus-intact oocytes with 10 times more mutant sperm insemination results in reduced fertilization rate of 45.7%; this indicates that sperm have defects in zona pellucida binding and oolemma fusion but are able to produce viable offspring
• sperm exhibit impaired zona pellucida binding; in IVF with cumulus-removed oocytes, a reduced number of spermatozoa binds the zona pellucida (ZP)

cellular
• sperm exhibit abnormal head morphology, with sperm heads lacking the hook shape




Genotype
MGI:8325063
cx2
Allelic
Composition
Slc35g3em1Osb/Slc35g3em1Osb
Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0
Genetic
Background
involves: C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Slc35g3em1Osb mutation (0 available); any Slc35g3 mutation (20 available)
Tg(CAG-RFP,Acr-EGFP)RBGS002Osb mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• sperm migration to the oviduct is impaired, with sperm found in the uterus but not in the oviduct, indicating defective utero-tubal junction migration

reproductive system
• sperm migration to the oviduct is impaired, with sperm found in the uterus but not in the oviduct, indicating defective utero-tubal junction migration





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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
05/12/2026
MGI 6.24
The Jackson Laboratory