C57BL/6N-Lamb3tm1c(KOMP)Wtsi/H
Status | Available to order |
EMMA ID | EM:10467 |
International strain name | C57BL/6N-Lamb3tm1c(KOMP)Wtsi/H |
Alternative name | EPD0079_6_C12 |
Strain type | Targeted Mutant Strains : Targeted Conditional |
Allele/Transgene symbol | Lamb3tm1c(KOMP)Wtsi |
Gene/Transgene symbol | Lamb3 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This line originates from KOMP ES clone EPD0079_6_C12, after breeding with a Flp recombinase deleter line to convert the original targeted allele tm1a (knock-out first allele) into a conditional allele tm1c. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Hypoplastic amelogenesis imperfecta / Orphanet_100031
- Junctional epidermolysis bullosa, generalized intermediate / Orphanet_79402
- Junctional epidermolysis bullosa, generalized severe / Orphanet_79404
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal tongue epithelium morphology / MGI
- blistering / MGI
- decreased body weight / MGI
- abnormal skin morphology / MGI
- abnormal nasopharynx morphology / MGI
- abnormal oropharynx morphology / MGI
- abnormal skin appearance / MGI
- postnatal lethality, complete penetrance / MGI
- neonatal lethality, complete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- abnormal epidermal-dermal junction morphology / MGI
- dermal-epidermal separation / MGI
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