- vasculature congestion / MGI
- abnormal vascular development / MGI
- abnormal angiogenesis / MGI
- decreased cell proliferation / MGI
- decreased body length / MGI
- decreased body weight / MGI
- polyphagia / MGI
- internal hemorrhage / MGI
- abnormal somite development / MGI
- decreased embryo size / MGI
- pale yolk sac / MGI
- embryonic growth arrest / MGI
- postnatal growth retardation / MGI
- abnormal lymphatic vessel morphology / MGI
- hemorrhage / MGI
- neoplasm / MGI
- increased circulating insulin level / MGI
- abnormal retinal vasculature morphology / MGI
- no phenotypic analysis / MGI
- abnormal vitelline vasculature morphology / MGI
- increased pancreatic beta cell number / MGI
- decreased lean body mass / MGI
- abnormal endocardium morphology / MGI
- embryonic growth retardation / MGI
- abnormal vitelline vascular remodeling / MGI
- fetal growth retardation / MGI
- decreased incidence of tumors by chemical induction / MGI
- abnormal anterior cardinal vein morphology / MGI
- abnormal dorsal aorta morphology / MGI
- decreased skeletal muscle mass / MGI
- abnormal brain vasculature morphology / MGI
- impaired glucose tolerance / MGI
- insulin resistance / MGI
- abnormal cell physiology / MGI
- increased circulating leptin level / MGI
- increased fat cell size / MGI
- abnormal lymphangiogenesis / MGI
- mortality/aging / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- chylous ascites / MGI
- abnormal intersomitic vessel morphology / MGI
- abnormal perineural vascular plexus morphology / MGI
B6.129P2-Pik3catm3Bvan/Orl
Status | Available to order |
EMMA ID | EM:11394 |
Citation information | RRID:IMSR_EM:11394 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 | B6.129P2-Pik3catm3Bvan/Orl |
Alternative name | B6.129P2-Pik3catm1Bvan/J |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Pik3catm3Bvan |
Gene/Transgene symbol | Pik3ca |
Information from provider
Provider | Bart Vanhaesebroeck |
Provider affiliation | UCL Cancer Institute, University College London |
Additional owner | the University of Edinburgh |
Genetic information | Exons 18 and 19 of the Pik3ca (PIK3CA/p110alpha) gene are flanked by loxP sites; backcrossed to C57BL/6J background. |
Phenotypic information | Homozygous:Mice are phenotypically normal.Heterozygous:Mice are phenotypically normal. |
Breeding history | Backcrossed to C57BL/6J for more than 10 generations. |
References |
|
Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Macrodactyly of toes, unilateral / Orphanet_295243
- Adult hepatocellular carcinoma / Orphanet_210159
- Hemimegalencephaly / Orphanet_99802
- Hemihyperplasia-multiple lipomatosis syndrome / Orphanet_276280
- Segmental progressive overgrowth syndrome with fibroadipose hyperplasia / Orphanet_314662
- CLOVES syndrome / Orphanet_140944
- Megalencephaly-capillary malformation-polymicrogyria syndrome / Orphanet_60040
- Macrodactyly of fingers, unilateral / Orphanet_295239
- Cowden syndrome / Orphanet_201
- Meningioma / Orphanet_2495
MGI phenotypes (gene matching)
Literature references
- Angiogenesis selectively requires the p110alpha isoform of PI3K to control endothelial cell migration.;Graupera Mariona, Guillermet-Guibert Julie, Foukas Lazaros C, Phng Li-Kun, Cain Robert J, Salpekar Ashreena, Pearce Wayne, Meek Stephen, Millan Jaime, Cutillas Pedro R, Smith Andrew J H, Ridley Anne J, Ruhrberg Christiana, Gerhardt Holger, Vanhaesebroeck Bart, ;2008;Nature;453;662-6; 18449193
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