- 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 |
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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