- hydronephrosis / MGI
- abnormal forelimb morphology / MGI
- abnormal liver development / MGI
- small liver / MGI
- enlarged liver sinusoidal spaces / MGI
- abnormal myogenesis / MGI
- abnormal muscle development / MGI
- thin diaphragm muscle / MGI
- abnormal tongue morphology / MGI
- small cerebellum / MGI
- abnormal motor neuron innervation pattern / MGI
- abnormal somatic motor system morphology / MGI
- impaired coordination / MGI
- decreased embryo size / MGI
- abnormal placenta development / MGI
- decreased trophoblast giant cell number / MGI
- abnormal placenta labyrinth morphology / MGI
- postnatal growth retardation / MGI
- increased mammary adenocarcinoma incidence / MGI
- respiratory failure / MGI
- neoplasm / MGI
- increased tumor incidence / MGI
- increased sarcoma incidence / MGI
- increased carcinoma incidence / MGI
- premature death / MGI
- no abnormal phenotype detected / MGI
- abnormal diaphragm morphology / MGI
- glomerulonephritis / MGI
- no phenotypic analysis / MGI
- abnormal muscle precursor cell migration / MGI
- hypaxial muscle hypoplasia / MGI
- decreased liver weight / MGI
- nervous system phenotype / MGI
- abnormal axon extension / MGI
- increased hemangiosarcoma incidence / MGI
- diaphragmatic hernia / MGI
- chromosome breakage / MGI
- abnormal tongue muscle morphology / MGI
- abnormal fetal growth/weight/body size / MGI
- decreased fetal size / MGI
- increased squamous cell carcinoma incidence / MGI
- small placenta / MGI
- pale placenta / MGI
- abnormal neuron physiology / MGI
- decreased skeletal muscle mass / MGI
- absent skeletal muscle / MGI
- muscle phenotype / MGI
- embryo phenotype / MGI
- abnormal liver parenchyma morphology / MGI
- increased histiocytic sarcoma incidence / MGI
- paraparesis / MGI
- reduced cerebellar foliation / MGI
- decreased tongue size / MGI
- abnormal neuron differentiation / MGI
- decreased lung tumor incidence / MGI
- increased mammary gland tumor incidence / MGI
- mortality/aging / MGI
- neonatal lethality, complete penetrance / MGI
- prenatal lethality, complete penetrance / MGI
- embryonic lethality between implantation and somite formation, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- absent diaphragm / MGI
- increased myoepithelioma incidence / MGI
- abnormal diaphragm development / MGI
- increased lymphoma incidence / MGI
- abnormal intrinsic tongue muscle morphology / MGI
C57BL/6N-Mettm2(MET*)Tcre/Cnrm
Status | Available to order |
EMMA ID | EM:13663 |
International strain name | C57BL/6N-Mettm2(MET*)Tcre/Cnrm |
Alternative name | Ex14Del-ki |
Strain type | Targeted Mutant Strains : Knock-in |
Allele/Transgene symbol | Mettm2(MET*)Tcre |
Gene/Transgene symbol | Met |
Information from provider
Provider | PAOLO COMOGLIO |
Provider affiliation | IFOM - Istituto FIRC di Oncologia Molecolare |
Additional owner | Tiziana Crepaldi, Ph.D., Department of Oncology, University of Turin, Candiolo Cancer Institute, Candiolo (Torino) ITALY |
Genetic information | Ex14Del-ki mice harbour the "humanized" knock-in mutation of the human MET allele without exon 14, which replaces the mouse Met gene. The coding region of exon 3 plus partial intron 3 was replaced with the mutant human MET CDS without exon 14 (NM_000245.4; 4032 bp). C57BL/6N ES cells were used for gene targeting. |
Phenotypic information | Homozygous:not knownHeterozygous:Mice heterozygous for the Ex14Del-ki allele are viable and fertile. |
Breeding history | The Ex14Del-ki mice were bred with C57BL/6N to generate the heterozygous mice. |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Pediatric hepatocellular carcinoma / Orphanet_33402
- Papillary renal cell carcinoma / Orphanet_319298
- Osteofibrous dysplasia / Orphanet_488265
- Autosomal recessive non-syndromic sensorineural deafness type DFNB / Orphanet_90636
- Hereditary papillary renal cell carcinoma / Orphanet_47044
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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