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Phenotypes Associated with This Genotype
Genotype
MGI:2654783
Allelic
Composition
Axltm1Grl/Axltm1Grl
Tyro3tm1Grl/Tyro3tm1Grl
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Axltm1Grl mutation (2 available); any Axl mutation (58 available)
Tyro3tm1Grl mutation (1 available); any Tyro3 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
N
• double mutant Sertoli cells exhibit normal phagocytosis of apoptotic spermatogenic cells relative to wild-type controls, as determined by lipid droplet formation using Oil Red O staining
• defects less severe than in mice homozygous for both Mertktm1Grl and Tyro3tm1Grl
• first estrus, which is dependent on a normal GnRH-induced LH surge mechanism, is delayed
• in contrast, onset of vaginal opening is normal
• double homozygous females display a delayed first estrus by 4 days relative to wild-type controls
• however, double homozygous females are fertile and deliver healthy litters of normal-size pups
• at 2 months of age, many double homozygous females exhibit decreased diestrous phase lengths relative to wild-type controls
• at 2 months of age, many double homozygous females spend more than twice as much time in proestrus than wild-type controls
• at 2-, 4-, and 6 months of age, double homozygous females exhibit prolonged irregular estrous cycle lengths, averaging ~2 to 3 times longer than those of age-matched wild-type controls

endocrine/exocrine glands

immune system

cellular
• double homozygous females exhibit increased cell death in the nose and dorsal forebrain relative to wild-type controls
• at E15, caspase 3 cleavage analysis revealed a 1.8-fold increase in the number of apoptotic cells in the dorsal forebrain, consistent with the location of loss of GnRH neurons number during migration
• at E15, double homozygous females show a 36% deficit in the appropriate targeting and positioning of GnRH neurons in the ventral forebrain

nervous system
• at E15, caspase 3 cleavage analysis revealed a 1.8-fold increase in the number of apoptotic cells in the dorsal forebrain, consistent with the location of loss of GnRH neurons number during migration
• at E15, double homozygous females show a 36% deficit in the appropriate targeting and positioning of GnRH neurons in the ventral forebrain
• at 2 months of age, double homozygous females show a 24% decrease in the total number of gonadotropin-releasing hormone (GnRH) neurons in the hypothalamus relative to wild-type controls
• a more striking deficit (34%) of GnRH neurons is noted in regions surrounding the organum vasculosum of the lamina terminalis (OVLT), known to be critical for the GnRH-induced LH surge
• at E15, double mutant brains show a striking loss (36%) of GnRH-immunoreactive cells within the context of ventral forebrain but not more rostrally


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
04/30/2024
MGI 6.23
The Jackson Laboratory