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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Dnajc3tm8663Wcl
targeted mutation 8663, Warren C Ladiges
MGI:3578105
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Dnajc3tm8663Wcl/Dnajc3tm8663Wcl C57BL/6-Dnajc3tm8663Wcl/Mmmh MGI:3578424
cx2
Dnajc3tm8663Wcl/Dnajc3tm8663Wcl
Sil1Gt(RST462)Byg/Sil1Gt(RST462)Byg
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J MGI:4417866


Genotype
MGI:3578424
hm1
Allelic
Composition
Dnajc3tm8663Wcl/Dnajc3tm8663Wcl
Genetic
Background
C57BL/6-Dnajc3tm8663Wcl/Mmmh
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dnajc3tm8663Wcl mutation (1 available); any Dnajc3 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygous null males have an average life span of 14.5 months compared to 25 months in wildtype, while females live longer although life span has not been determined

growth/size/body
• homozygous null mice are smaller as early as 2 weeks of age, and growth curves show that body weights increase in parallel over time but never catch up to that of heterozygotes or wildtype

adipose tissue
• 10-12 month old homozygous null males have an average of 7% body fat compared to 34% in wildtype

homeostasis/metabolism
• higher serum glucose levels, however homozygous null mice are not insulin resistant
• at 4 months of age, began to increase water intake with subsequent increase in urination and evidence of glucosuria, however no evidence of urine ketones

renal/urinary system
• at 4 months of age, began to increase water intake with subsequent increase in urination and evidence of glucosuria, however no evidence of urine ketones

endocrine/exocrine glands
• cytoplasmic atrophy and collapse within the pancreatic islets and multifocal areas of cytoplasmic clefts and apoptotic bodies were seen in islets of 6-month old homozygous null males, however no differences in acini or other parenchyma
• the mass of insulin-producing cells was significantly decreased in islets
• insulin-producing beta cells, but not glucagons producing cells, were greatly depleted in pancreatic islets that was associated with increased apoptosis in islets

behavior/neurological
• increased consumption of food (4.4 grams of food per gram of body weight compared to 2.8 and 3 grams of food per gram body weight in wildtype and heterozygotes, respectively)




Genotype
MGI:4417866
cx2
Allelic
Composition
Dnajc3tm8663Wcl/Dnajc3tm8663Wcl
Sil1Gt(RST462)Byg/Sil1Gt(RST462)Byg
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dnajc3tm8663Wcl mutation (1 available); any Dnajc3 mutation (25 available)
Sil1Gt(RST462)Byg mutation (0 available); any Sil1 mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• at 20 weeks, mice exhibit a normal rear stance width unlike Sil1Gt(RST462)Byg homozygotes

nervous system
• at 4 months of age, mice begin to exhibit Purkinje cell degeneration
• however, by 8 months most Purkinje cells remain intact and few Purkinje cells exhibit ubiquitin+ inclusions





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory