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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Del(7Ube3a-Snrpn)1Alb
deletion, Chr 7, Arthur L Beaudet 1
MGI:2384048
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Del(7Ube3a-Snrpn)1Alb/+ involves: 129S7/SvEvBrd * C57BL/6J MGI:3662872


Genotype
MGI:3662872
ht1
Allelic
Composition
Del(7Ube3a-Snrpn)1Alb/+
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• majority of pups with paternally-derived deletion of the region die in the neonatal period
• 50% of paternal heterozygotes die by day 12 and 78% die before weaning
• when males with the maternally-inherited deletion are crossed to C57BL/6J males, ~80% lethality is observed

growth/size/body
• ~50% of offspring of male chimeras mated to wild-type C57BL/6J females are runted and relatively weak; these pups inherited the deletion from chimeric male parent
• pups inheriting the deletion paternally exhibit severe growth retardation compared to controls
• affected pups are underweight (1.18g at 6-12 hours of age) vs wild-type (1.36g)

behavior/neurological
• pups inheriting the deletion paternally are able to suckle but amount of milk in stomachs is less than in wild-type controls
• pups inheriting the deletion paternally display an impaired righting response when placed on their backs
• pups inheriting the deletion paternally exhibit decreased movement

muscle
• pups inheriting the deletion paternally display hypotonia

normal phenotype
• pups inheriting the deletion from the female parent are normal and viable (ie pups from female chimeras bred to wild-type C57BL/6J males)





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last database update
10/09/2024
MGI 6.24
The Jackson Laboratory