- embryonic growth retardation / MGI
- prenatal lethality, complete penetrance / MGI
- abnormal vascular development / MGI
- pale yolk sac / MGI
- pericardial edema / MGI
- abnormal vitelline vascular remodeling / MGI
- abnormal anterior cardinal vein morphology / MGI
- abnormal dorsal aorta morphology / MGI
- hemopericardium / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal perineural vascular plexus morphology / MGI
- absent lymphatic vessels / MGI
B6.129-Flt4tm1Ali/Oulu
Status | Available to order |
EMMA ID | EM:10724 |
Citation information | RRID:IMSR_EM:10724 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 | B6.129-Flt4tm1Ali/Oulu |
Alternative name | VEGFR3/LacZ |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Flt4tm1Ali |
Gene/Transgene symbol | Flt4 |
Information from provider
Provider | Kari Alitalo |
Provider affiliation | Translational Cancer Biology Research Program; Institute of Biomedicine, University of Helsinki |
Genetic information | Vegfr3 has been replaced with LacZ-insert. |
Phenotypic information | Homozygous:Homozygous mice die around E10-E11 because of the cardiovascular defectsHeterozygous:No obvious phenotype |
Breeding history | 10 backcrosses to C57BL/6 |
References |
|
Homozygous fertile | no |
Homozygous viable | no |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | University of Oulu, Oulu, Finland |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Tetralogy of Fallot / Orphanet_3303
- Milroy disease / Orphanet_79452
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal adipose tissue distribution / MGI
- abnormal vascular development / MGI
- abnormal intestine morphology / MGI
- abnormal liver morphology / MGI
- thick dermal layer / MGI
- pale yolk sac / MGI
- edema / MGI
- pericardial edema / MGI
- abnormal lymphatic vessel morphology / MGI
- postnatal lethality / MGI
- no abnormal phenotype detected / MGI
- hydrops fetalis / MGI
- no phenotypic analysis / MGI
- extremity edema / MGI
- lymphedema / MGI
- abnormal lymph circulation / MGI
- embryonic growth retardation / MGI
- abnormal vitelline vascular remodeling / MGI
- abnormal anterior cardinal vein morphology / MGI
- abnormal dorsal aorta morphology / MGI
- hemopericardium / MGI
- cardiovascular system phenotype / MGI
- reproductive system phenotype / MGI
- abnormal lymphangiogenesis / MGI
- absent lymphatic vessels / MGI
- neonatal lethality, complete penetrance / MGI
- prenatal lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- chylous ascites / MGI
- abnormal perineural vascular plexus morphology / MGI
Literature references
- Cardiovascular failure in mouse embryos deficient in VEGF receptor-3.;Dumont D J, Jussila L, Taipale J, Lymboussaki A, Mustonen T, Pajusola K, Breitman M, Alitalo K, ;1998;Science (New York, N.Y.);282;946-9; 9794766
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