STOCK Ptentm Tg(Alb1-cre) Tg(Alb1-HCVN)35Sml/Orl
Status | Available to order |
EMMA ID | EM:11052 |
International strain name | STOCK Ptentm Tg(Alb1-cre) Tg(Alb1-HCVN)35Sml/Orl |
Alternative name | HCV +/+ AlbCRE +/+ PTEN flox/flox |
Strain type | Transgenic Strains |
Allele/Transgene symbol | Tg(Alb1-cre) |
Gene/Transgene symbol | Tg(Alb1-cre) |
Information from provider
Provider | Hervé LERAT |
Provider affiliation | Equipe 18, IMRB, Inserm U955 |
Genetic information | These mice are conditionally invalidated for PTEN (Exon 4 and 5 floxed), they are transgenic for cre recombinase (albumin promoter) and transgenic for the full hepatitis C virus (HCV) ORF (Albumin promoter). They were generated by crossing FL-N/35 mice with PTEN flox/flox and Alb CRE+/+ mice. These mice are invalidated for PTEN in their liver and express all HCV proteins (genotype 1b) in their liver. |
Phenotypic information | Homozygous:Severe non-alcoholic steatohepatitis (NASH) and hepatocellular carcinoma (HCC)Heterozygous:Severe NASH and HCC |
References | None available |
Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | yes |
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
- Squamous cell carcinoma of salivary glands / Orphanet_500481
- Squamous cell carcinoma of the oral cavity / Orphanet_502363
- Squamous cell carcinoma of the larynx / Orphanet_494550
- Squamous cell carcinoma of the oropharynx / Orphanet_500478
- Squamous cell carcinoma of the nasal cavity and paranasal sinuses / Orphanet_500464
- Squamous cell carcinoma of the hypopharynx / Orphanet_494547
- Squamous cell carcinoma of the lip / Orphanet_502366
- Activated PI3K-delta syndrome / Orphanet_397596
- Lhermitte-Duclos disease / Orphanet_65285
- Cowden syndrome / Orphanet_201
- Bannayan-Riley-Ruvalcaba syndrome / Orphanet_109
- Macrocephaly-intellectual disability-autism syndrome / Orphanet_210548
- Proteus-like syndrome / Orphanet_2969
- Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome / Orphanet_137608
- Proteus syndrome / Orphanet_744
- Bilateral frontoparietal polymicrogyria / Orphanet_101070
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