- increased leukocyte cell number / MGI
- increased neutrophil cell number / MGI
- abnormal intestinal epithelium morphology / MGI
- crypts of Lieberkuhn abscesses / MGI
- abnormal intestinal mucosa morphology / MGI
- small spleen / MGI
- spleen hypoplasia / MGI
- impaired hematopoiesis / MGI
- abnormal humoral immune response / MGI
- decreased IgG level / MGI
- decreased IgM level / MGI
- decreased IgA level / MGI
- intestinal inflammation / MGI
- decreased inflammatory response / MGI
- abnormal B cell differentiation / MGI
- small lymph nodes / MGI
- abnormal Peyer's patch germinal center morphology / MGI
- increased susceptibility to viral infection / MGI
- abnormal B cell physiology / MGI
- decreased immunoglobulin level / MGI
- increased IgE level / MGI
- no phenotypic analysis / MGI
- decreased susceptibility to induced arthritis / MGI
- decreased B-1 B cell number / MGI
- increased lymphocyte cell number / MGI
- decreased B cell number / MGI
- decreased B cell proliferation / MGI
- cardiovascular system phenotype / MGI
- immune system phenotype / MGI
- decreased B-1a cell number / MGI
- decreased marginal zone B cell number / MGI
- absent B-1 B cells / MGI
- decreased B-2 B cell number / MGI
- decreased mature B cell number / MGI
- absent spleen germinal center / MGI
- decreased IgG1 level / MGI
- decreased IgG2a level / MGI
- decreased IgG2b level / MGI
- decreased IgG3 level / MGI
- increased circulating interferon-alpha level / MGI
- abnormal platelet aggregation / MGI
- decreased response to antigen / MGI
- increased response to antigen / MGI
B6.Cg-Pik3cdtm1(S1039A)Bvan/Orl
Status | Available to order |
EMMA ID | EM:11502 |
Citation information | RRID:IMSR_EM:11502 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | B6.Cg-Pik3cdtm1(S1039A)Bvan/Orl |
Alternative name | p110delta PI3K S1039A |
Strain type | Targeted Mutant Strains : Point mutation |
Allele/Transgene symbol | Pik3cdtm1(S1039A)Bvan |
Gene/Transgene symbol | Pik3cd |
Information from provider
Provider | Bart Vanhaesebroeck |
Provider affiliation | UCL Cancer Institute, University College London |
Additional owner | Developed by the Ludwig Institute for Cancer Research (LICR). The materials are available to academic researchers. Commercial entity need to obtain a licensing agreement. |
Genetic information | Knock-in mice in which the endogenous PIK3CD/p110delta PI3K gene is mutated so that it now encodes a p110delta protein with S1039 mutated to alanine. |
Phenotypic information | Homozygous:viable - no phenotypes detectedHeterozygous:viable - no phenotypes detected |
Breeding history | Backcrossed onto C57BL/6J for more than 10 generations. |
References | None available |
Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | not known |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Activated PI3K-delta syndrome / Orphanet_397596
- Combined immunodeficiency with faciooculoskeletal anomalies / Orphanet_221139
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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