Phenotypes associated with this allele

• Allele Symbol: Tg(Igh-Lmp2a)13FRdni
• Allele Name: transgene insertion 13F, R D Nicholls
• Allele ID: MGI:3769767
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
tg1	Tg(Igh-Lmp2a)13FRdni/0	involves: C57BL/6 * CD-1 * SJL	MGI:3769776

Genotype
MGI:3769776

tg1

• Allelic Composition: Tg(Igh-Lmp2a)13FRdni/0
• Genetic Background: involves: C57BL/6 * CD-1 * SJL

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

mortality/aging

postnatal lethality ( J:56614 )

• when this allele is inherited paternally, mice die within a week of birth

• however, when this allele is inherited maternally mice are normal

homeostasis/metabolism

dehydration ( J:56614 )

• when this allele is inherited paternally, mice exhibit dehydration despite milk in their stomachs

behavior/neurological

decreased locomotor activity ( J:56614 )

• when this allele is inherited paternally, mice exhibit reduced movement compared to wild-type mice

respiratory system

abnormal respiration ( J:56614 )

• when this allele is inherited paternally, mice exhibit irregular breathing

cellular

maternal imprinting ( J:56614 )

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
Prader-Willi syndrome		DOID:11983	OMIM:176270	J:56614