B6;Cg-Pmeltm1.1(cre/ERT2)Jkn/H
Status | Available to order |
EMMA ID | EM:13225 |
International strain name | B6;Cg-Pmeltm1.1(cre/ERT2)Jkn/H |
Alternative name | Pmel-CMN |
Strain type | Targeted Mutant Strains : Knock-in |
Allele/Transgene symbol | Pmeltm1.1(cre/ERT2)Jkn |
Gene/Transgene symbol | Pmel |
Information from provider
Provider | Richard Mort |
Provider affiliation | Biomedical and Life Sciences, Lancaster University |
Additional owner | Frank Constantini's group developed the R26YFPR allele but widely available. |
Genetic information | Pmel-CMN mice carry a knock-in cassette replacing the STOP codon of the Pmel gene with creERT2-2a-marcks-mKate-2a-H2BCerulean. |
Phenotypic information | Homozygous:No phenotype.Heterozygous:No phenotype. |
Breeding history | Pmel-CMN generated in E14 129P2/OlaHsd ES cells. Outcrossed to C57BL/6. |
References |
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Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- diluted coat color / MGI
- irregular coat pigmentation / MGI
- pigmentation phenotype / MGI
- no phenotypic analysis / MGI
- abnormal melanosome morphology / MGI
- homeostasis/metabolism phenotype / MGI
- hematopoietic system phenotype / MGI
- reduced hair shaft melanin granule number / MGI
- abnormal tail hair pigmentation / MGI
- abnormal retinal melanin granule morphology / MGI
- abnormal choroid melanin granule morphology / MGI
Literature references
- Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2-mediated recombination in the melanocyte lineage.;Wilkinson Emma L, Brennan Louise C, Harrison Olivia J, Crane-Smith Zoe, Gautier Philippe, Keighren Margaret A, Budd Peter, Swaminathan Karthic, Machesky Laura M, Allinson Sarah L, Jackson Ian J, Mort Richard L, ;2023;Pigment cell & melanoma research;36;71-77; 36412082
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