C57BL/6NTac-Tmem94tm1c(EUCOMM)Wtsi/IcsOrl
Status | Available to order |
EMMA ID | EM:15448 |
Citation information | RRID:IMSR_EM:15448 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 | C57BL/6NTac-Tmem94tm1c(EUCOMM)Wtsi/IcsOrl |
Alternative name | C57BL/6NTac-Tmem94tm1c(EUCOMM)Wtsi/IcsOrl |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Tmem94tm1c(EUCOMM)Wtsi |
Gene/Transgene symbol | Tmem94 |
Information from provider
Provider | Cécile FREMOND |
Provider affiliation | CNRS-TAAM-UAR44 |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0215_1_D09. For further details on the construction of this clone see the page at the IMPC portal. Mice carrying the Tmem94-tm1a(EUCOMM)Wtsi allele have been crossed to flp expressing mice (B6N Gt(ROSA)26Sor-tm2(CAG-flpo,-EYFP)Ics) to obtain the Tmem94-tm1c(EUCOMM)Wtsi allele. |
Phenotypic information | Homozygous:Homozygous mice have not been generated.Heterozygous:We did not observe any significant phenotype. |
Breeding history | Rederived mice carrying the Tmem94tm1a(EUCOMM)Wtsi allele, were crossed to flp recombinase deleter mice (B6N Gt(ROSA)26Sortm2(CAG-flpo,-EYFP)Ics, EMMA strain EM:05490) to obtain the Tmem94tm1c(EUCOMM)Wtsi allele. |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- TMEM94-associated congenital heart defect-facial dysmorphism-developmental delay syndrome / Orphanet_562569
IMPC phenotypes (gene matching)
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