B6.129P2-Pik3catm3Bvan/Orl
Status | Available to order |
EMMA ID | EM:11394 |
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 |
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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
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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