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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Prkcdtm1Kin
targeted mutation 1, Kei-ichi Nakayama
MGI:2179710
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Prkcdtm1Kin/Prkcdtm1Kin involves: 129P2/OlaHsd MGI:3841727
hm2
Prkcdtm1Kin/Prkcdtm1Kin involves: 129P2/OlaHsd * C57BL/6 MGI:3841648
cx3
Blnktm1Dkit/Blnktm1Dkit
Prkcdtm1Kin/Prkcdtm1Kin
involves: 129P2/OlaHsd * C57BL/6 * NZB MGI:3841693


Genotype
MGI:3841727
hm1
Allelic
Composition
Prkcdtm1Kin/Prkcdtm1Kin
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prkcdtm1Kin mutation (1 available); any Prkcd mutation (54 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• as determined by marker expression, osteoblast differentiation is impeded compared to in wild-type mice
• at E13.5, cultured limb priomordial cells produce fewer bone nodules and more cartilage nodules than formed by wild-type cells
• at E15.5, mice exhibit less ossification compared to wild-type mice
• at E15.5, mineralization of the maxilla and mandible is minimal compared to in wild-type mice
• at E14.5 and E15.5, bone collars of ossifying skeletal elements, specifically long bones, are shorter than in wild-type mice

cellular
• as determined by marker expression, osteoblast differentiation is impeded compared to in wild-type mice
• at E13.5, cultured limb priomordial cells produce fewer bone nodules and more cartilage nodules than formed by wild-type cells




Genotype
MGI:3841648
hm2
Allelic
Composition
Prkcdtm1Kin/Prkcdtm1Kin
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prkcdtm1Kin mutation (1 available); any Prkcd mutation (54 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• in response to F(ab)s specific for IgM and antibodies to CD40 or LSP (J:76135)
• when transferred into Rag null mice, more B220+ IgM+ cells compared to when wild-type cells are transplanted (J:76135)
• when stimulated with anti-CD40 antibodies or anti-IgM antibodies (J:143854)
• anti-CD40- and IL4-stimulated splenic B cells exhibit enhanced differentiation into IgG producing plasma cells compared to in wild-type mice
• the number of IgM+ TCR(beta)- B220+ cells are increased in the spleen and lymph nodes compared to in wild-type mice
• however, the numbers of splenic and peritoneal CD5+ B lymphocytes are normal
• when transferred into Rag null mice, more B220+ IgM+ cells compared to when wild-type cells are transplanted
• T1 and T2 B cells are increased 2- to 3-fold compared to in wild-type mice
• increased compared to in wild-type mice
• increased compared to in wild-type mice
• from stimulated B cells
• perivascular infiltration of leukocytes, comprised mostly of B cells, is observed in the kidney, liver, lungs, and salivary glands unlike in wild-type mice
• glomeruli are enlarged and stain positive for IgG and C3 in the mesangial region and along capillary walls unlike in wild-type mice

renal/urinary system
• glomeruli are enlarged and stain positive for IgG and C3 in the mesangial region and along capillary walls unlike in wild-type mice

endocrine/exocrine glands
• the total number of insulin granules is greater than in wild-type beta-cells
• following glucose treatment, the number of granules within 100 nm or 100-200 nm from the plasma membrane is increased compared to in wild-type beta-cells
• mice exhibit reduced glucose-stimulated insulin secretion compared to in wild-type mice
• islet cells stimulated with glucose-, KCl-, or phorbol 12-myristate 13-acetate with or without forskolin exhibit decreased insulin secretion compared to in wild-type cells

growth/size/body

hematopoietic system
• in response to F(ab)s specific for IgM and antibodies to CD40 or LSP (J:76135)
• when transferred into Rag null mice, more B220+ IgM+ cells compared to when wild-type cells are transplanted (J:76135)
• when stimulated with anti-CD40 antibodies or anti-IgM antibodies (J:143854)
• anti-CD40- and IL4-stimulated splenic B cells exhibit enhanced differentiation into IgG producing plasma cells compared to in wild-type mice
• the number of IgM+ TCR(beta)- B220+ cells are increased in the spleen and lymph nodes compared to in wild-type mice
• however, the numbers of splenic and peritoneal CD5+ B lymphocytes are normal
• when transferred into Rag null mice, more B220+ IgM+ cells compared to when wild-type cells are transplanted
• T1 and T2 B cells are increased 2- to 3-fold compared to in wild-type mice

homeostasis/metabolism
• mice exhibit reduced glucose-stimulated insulin secretion compared to in wild-type mice
• islet cells stimulated with glucose-, KCl-, or phorbol 12-myristate 13-acetate with or without forskolin exhibit decreased insulin secretion compared to in wild-type cells
• from 8 to 20 weeks with no decrease in insulin sensitivity

cellular
• in response to F(ab)s specific for IgM and antibodies to CD40 or LSP (J:76135)
• when transferred into Rag null mice, more B220+ IgM+ cells compared to when wild-type cells are transplanted (J:76135)
• when stimulated with anti-CD40 antibodies or anti-IgM antibodies (J:143854)




Genotype
MGI:3841693
cx3
Allelic
Composition
Blnktm1Dkit/Blnktm1Dkit
Prkcdtm1Kin/Prkcdtm1Kin
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * NZB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Blnktm1Dkit mutation (1 available); any Blnk mutation (78 available)
Prkcdtm1Kin mutation (1 available); any Prkcd mutation (54 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• mice exhibit poor response to anti-IgM antibodies or LPS but a stronger than normal response to anti-CD40 antibodies
• anti-CD40- and IL4-stimulated splenic B cells exhibit moderately enhanced differentiation into IgG producing plasma cells compared to in wild-type mice
• as in Blnktm1Dkit homozygotes
• in the peritoneal cavity
• in the peritoneal cavity
• higher than in Blnktm1Dkit homozygotes
• higher than in Blnktm1Dkit homozygotes
• higher than in Blnktm1Dkit homozygotes
• 10-fold higher than in Blnktm1Dkit homozygotes
• 10-fold higher than in Blnktm1Dkit homozygotes

hematopoietic system
• mice exhibit poor response to anti-IgM antibodies or LPS but a stronger than normal response to anti-CD40 antibodies
• anti-CD40- and IL4-stimulated splenic B cells exhibit moderately enhanced differentiation into IgG producing plasma cells compared to in wild-type mice
• as in Blnktm1Dkit homozygotes
• in the peritoneal cavity
• in the peritoneal cavity
• higher than in Blnktm1Dkit homozygotes
• higher than in Blnktm1Dkit homozygotes
• higher than in Blnktm1Dkit homozygotes
• 10-fold higher than in Blnktm1Dkit homozygotes
• 10-fold higher than in Blnktm1Dkit homozygotes

cellular
• mice exhibit poor response to anti-IgM antibodies or LPS but a stronger than normal response to anti-CD40 antibodies





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory