About   Help   FAQ
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 (52 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 (52 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 (76 available)
Prkcdtm1Kin mutation (1 available); any Prkcd mutation (52 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





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/09/2024
MGI 6.23
The Jackson Laboratory