- short tibia / IMPC
- decreased prepulse inhibition / IMPC
- decreased mean corpuscular hemoglobin concentration / IMPC
- abnormal coat/ hair morphology / IMPC
- abnormal coat/hair pigmentation / IMPC
- decreased exploration in new environment / IMPC
- abnormal skin morphology / IMPC
- decreased locomotor activity / IMPC
- increased heart weight / IMPC
- increased fasting circulating glucose level / IMPC
- abnormal coat appearance / IMPC
- increased Ly6C-positive mature NK cell number / IMPC
- decreased NK cell number / IMPC
- increased circulating calcium level / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- increased CD11b-high dendritic cell number / IMPC
- decreased mean corpuscular volume / IMPC
- decreased hemoglobin content / IMPC
- increased effector memory CD8-positive, alpha-beta T cell number / IMPC
- immune system phenotype / IMPC
- decreased CD8-positive, alpha-beta T cell number / IMPC
- decreased hematocrit / IMPC
Tmprss6tm1b(EUCOMM)Wtsi/Ics
| Status | Available to order |
| EMMA ID | EM:16228 |
| Citation information | RRID:IMSR_EM:16228 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 | Tmprss6tm1b(EUCOMM)Wtsi/Ics |
| Alternative name | Tmprss6tm1b(EUCOMM)Wtsi/Ics |
| Strain type | Targeted Mutant Strains : Other targeted |
| Allele/Transgene symbol | Tmprss6tm1b(EUCOMM)Wtsi |
| Gene/Transgene symbol | Tmprss6 |
Information from provider
| Provider | ICS, Institut Clinique de la Souris |
| Provider affiliation | ICS, Institut Clinique de la Souris |
| Genetic information | Cre-mediated excision of the parental Tmprss6tm1a(EUCOMM)Wtsi allele resulted in the removal of the promoter-driven neomycin selection cassette and critical exon(s) leaving behind the inserted lacZ reporter sequence |
| Phenotypic information | Homozygous:N/AHeterozygous:N/A |
| Breeding history | 100% C57BL/6N (C57BL/6NCrl 74,61% C57BL/6NTac 25,39%) |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- IRIDA syndrome / Orphanet_209981
IMPC phenotypes (gene matching)
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