STOCK Rettm1.1Pern/Kctt
Status | Available to order |
EMMA ID | EM:02080 |
International strain name | STOCK Rettm1.1Pern/Kctt |
Alternative name | Ret flox |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Rettm1.1Pern, |
Gene/Transgene symbol | Ret |
Information from provider
Provider | Christel Baudet |
Provider affiliation | Universite Bordeaux 2 |
Genetic information | Two loxP sites flanking exons 12 and 13, with also an frt site in 3' resulting from the excision of the Neo cassette by Flpe. |
Phenotypic information | None. |
References |
|
Information from EMMA
Archiving centre | Karolinska Institutet, Stockholm, Sweden |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Renal agenesis, bilateral / Orphanet_1848
- Multiple endocrine neoplasia type 2B / Orphanet_247709
- Familial medullary thyroid carcinoma / Orphanet_99361
- Renal agenesis, unilateral / Orphanet_93100
- Haddad syndrome / Orphanet_99803
- Multiple endocrine neoplasia type 2A / Orphanet_247698
- Hirschsprung disease / Orphanet_388
Literature references
- Retrograde signaling onto Ret during motor nerve terminal maturation.;Baudet Christel, Pozas Ester, Adameyko Igor, Andersson Elisabet, Ericson Johan, Ernfors Patrik, ;2008;The Journal of neuroscience : the official journal of the Society for Neuroscience;28;963-75; 18216204
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