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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pigatm1Bsl
targeted mutation 1, Monica Bessler
MGI:2386121
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Pigatm1Bsl/Piga+
Tg(FES-cre)31Bsl/0
involves: 129S1/Sv * C57BL/6 * CBA/Ca MGI:3814205
cn2
Pigatm1Bsl/Y
Tg(FES-cre)31Bsl/0
involves: 129S1/Sv * C57BL/6 * CBA/Ca MGI:3814206
cn3
Pigatm1Bsl/Piga+
Tg(EIIa-cre)C5379Lmgd/0
involves: 129S1/Sv * FVB/NJ MGI:3814198


Genotype
MGI:3814205
cn1
Allelic
Composition
Pigatm1Bsl/Piga+
Tg(FES-cre)31Bsl/0
Genetic
Background
involves: 129S1/Sv * C57BL/6 * CBA/Ca
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pigatm1Bsl mutation (0 available); any Piga mutation (3 available)
Tg(FES-cre)31Bsl mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• developing around 12 months of age

behavior/neurological
• general muscular weakness after 12 months of age
• decreased overall activity after 12 months of age

neoplasm
• sometimes seen in spleen and lymph nodes at 12 months of age
• sometimes seen in spleen and lymph nodes at 12 months of age




Genotype
MGI:3814206
cn2
Allelic
Composition
Pigatm1Bsl/Y
Tg(FES-cre)31Bsl/0
Genetic
Background
involves: 129S1/Sv * C57BL/6 * CBA/Ca
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pigatm1Bsl mutation (0 available); any Piga mutation (3 available)
Tg(FES-cre)31Bsl mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• developing around 12 months of age

behavior/neurological
• general muscular weakness after 12 months of age
• wide gait in males only, after 12 months of age
• decreased overall activity after 12 months of age

neoplasm
• sometimes seen in spleen and lymph nodes at 12 months of age
• sometimes seen in spleen and lymph nodes at 12 months of age




Genotype
MGI:3814198
cn3
Allelic
Composition
Pigatm1Bsl/Piga+
Tg(EIIa-cre)C5379Lmgd/0
Genetic
Background
involves: 129S1/Sv * FVB/NJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pigatm1Bsl mutation (0 available); any Piga mutation (3 available)
Tg(EIIa-cre)C5379Lmgd mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• increased perinatal lethality

hematopoietic system
• high level of blood cells lacking glycosylphosphatidylinositol anchors
• level of RBC lacking glycosylphosphatidylinositol anchors highest at birth (up to 53%) and declining over 4 weeks to around 4%
• elevated numbers of reticulocytes
• RBC half life only 50% of normal
• increased susceptibility to lytic activity of activated complement

craniofacial
• orofacial abnormalities when cre recombination levels are highest
• when cre recombination levels are highest

behavior/neurological
• unable to suckle when cre recombination levels are highest

digestive/alimentary system
• when cre recombination levels are highest

growth/size/body
• orofacial abnormalities when cre recombination levels are highest
• when cre recombination levels are highest





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory