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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		Gba1tm3Ggb
targeted mutation 3, Gregory A Grabowski
MGI:2680324
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
 		Gba1tm3Ggb/Gba1tm3Ggb involves: 129S5/SvEvBrd MGI:2680502
ht2
 		Gba1tm3Ggb/Gba1tm1Nsb involves: 129S/SvEv * 129S5/SvEvBrd * C57BL/6 MGI:2680504


Genotype
MGI:2680502
hm1
Allelic
Composition		 Gba1tm3Ggb/Gba1tm3Ggb
Genetic
Background		 involves: 129S5/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gba1tm3Ggb mutation (0 available); any Gba1 mutation (43 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
cardiovascular system
abnormal pulmonary circulation ( J:86334 )
• small accumulations of glucosylceramide (2X wild-type values) at 6.5 months of age

hematopoietic system
abnormal spleen morphology ( J:86334 )
• small numbers of storage cells at 7 months of age
• small accumulations of glucsylceramide (2X wild-type values) at 6.5 months of age

immune system
abnormal spleen morphology ( J:86334 )
• small numbers of storage cells at 7 months of age
• small accumulations of glucsylceramide (2X wild-type values) at 6.5 months of age

liver/biliary system
abnormal liver physiology ( J:86334 )
• small accumulations of glucosylceramide (2X wild-type values) at 6.5 months of age

respiratory system
abnormal pulmonary circulation ( J:86334 )
• small accumulations of glucosylceramide (2X wild-type values) at 6.5 months of age

nervous system
abnormal brain morphology ( J:174780 )
• 42 week old mice exhibit accumulation of soluble and insoluble alpha-synuclein in the brain

Mouse Models of Human Disease
 DO ID OMIM ID(s) Ref(s)
Gaucher's disease DOID:1926 J:86334




Genotype
MGI:2680504
ht2
Allelic
Composition		 Gba1tm3Ggb/Gba1tm1Nsb
Genetic
Background		 involves: 129S/SvEv * 129S5/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gba1tm1Nsb mutation (2 available); any Gba1 mutation (43 available)
Gba1tm3Ggb mutation (0 available); any Gba1 mutation (43 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
cardiovascular system
abnormal pulmonary circulation ( J:86334 )
• small accumulations of glucosylceramide (2X wild-type values) at 6.5 months of age

hematopoietic system
abnormal spleen morphology ( J:86334 )
• small numbers of storage cells at 3-4 months of age
• small accumulations of glucosylceramide (2X wild-type values) at 6.5 months of age

immune system
abnormal spleen morphology ( J:86334 )
• small numbers of storage cells at 3-4 months of age
• small accumulations of glucosylceramide (2X wild-type values) at 6.5 months of age

liver/biliary system
abnormal liver physiology ( J:86334 )
• small accumulations of glucosylceramide (2X wild-type values) at 6.5 months of age

respiratory system
abnormal pulmonary circulation ( J:86334 )
• small accumulations of glucosylceramide (2X wild-type values) at 6.5 months of age

Mouse Models of Human Disease
 DO ID OMIM ID(s) Ref(s)
Gaucher's disease DOID:1926 J:86334




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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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory