mortality/aging
• 73% of mice survive to P18
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reproductive system
• many PGCs with abnormal morphology are retained in the hindgut at E10.5
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• moderate numbers of primordial germ cells (PGCs) are seen in genital ridges relative to wild-type and KitlSl-gb homozygotes at E11.5
• at E9.5, PGC numbers in the hindgut are 44% of wild-type
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• at E10.5, many PGCs in hindgut appear to be disintegrating; abnormal PGCs in hindgut tend to be nonmotile and apoptotic
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• at E10.5, only 50% of total PGCs have migrated from hindgut, compared to 93% in wild-type
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• proliferation indices of migratory (in mesentery and genital ridges) and postmigratory PGCs (in genital ridges) at 10.5 and 11.5 are significantly reduced compared to wild-type values (54-66% of wild-type values)
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pigmentation
• some animals have pigmented patches on their heads
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hematopoietic system
• severe at birth
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• significantly lower than wild-type at birth (34% of wild-type value)
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• significantly lower than wild-type at P24-25
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• significantly increased compared to wild-type at P24-25
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• increased compared to wild-type at P24-25
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• significantly increased compared to wild-type at P24-25
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cellular
• many PGCs with abnormal morphology are retained in the hindgut at E10.5
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• moderate numbers of primordial germ cells (PGCs) are seen in genital ridges relative to wild-type and KitlSl-gb homozygotes at E11.5
• at E9.5, PGC numbers in the hindgut are 44% of wild-type
|
• at E10.5, many PGCs in hindgut appear to be disintegrating; abnormal PGCs in hindgut tend to be nonmotile and apoptotic
|
• at E10.5, only 50% of total PGCs have migrated from hindgut, compared to 93% in wild-type
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• proliferation indices of migratory (in mesentery and genital ridges) and postmigratory PGCs (in genital ridges) at 10.5 and 11.5 are significantly reduced compared to wild-type values (54-66% of wild-type values)
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integument
• some animals have pigmented patches on their heads
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