- increased circulating calcium level / IMPC
- decreased hematocrit / IMPC
- abnormal coat/ hair morphology / IMPC
- decreased locomotor activity / IMPC
- decreased exploration in new environment / IMPC
- abnormal coat appearance / IMPC
- abnormal skin morphology / IMPC
- abnormal coat/hair pigmentation / IMPC
- decreased mean corpuscular volume / IMPC
- short tibia / IMPC
- increased heart weight / IMPC
- decreased hemoglobin content / IMPC
- immune system phenotype / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- decreased mean corpuscular hemoglobin concentration / IMPC
- decreased NK cell number / IMPC
- decreased CD8-positive, alpha-beta T cell number / IMPC
- decreased prepulse inhibition / IMPC
- increased effector memory CD8-positive, alpha-beta T cell number / IMPC
- increased fasting circulating glucose level / IMPC
- increased CD11b-high dendritic cell number / IMPC
- increased Ly6C-positive mature NK cell number / IMPC
C57BL/6N-Tmprss6tm1b(EUCOMM)Wtsi/Ics
| Status | Under development - register interest |
| EMMA ID | EM:16702 |
| Citation information | RRID:IMSR_EM:16702 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/6N-Tmprss6tm1b(EUCOMM)Wtsi/Ics |
| Alternative name | EPD0453_1_B07 |
| Strain type | Targeted Mutant Strains |
| Allele/Transgene symbol | Tmprss6tm1b(EUCOMM)Wtsi |
| Gene/Transgene symbol | Tmprss6 |
| Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
| Provider | ICS, Institut Clinique de la Souris |
| Provider affiliation | ICS, Institut Clinique de la Souris |
| Genetic information | This mouse line originates from EUCOMM ES clone EPD0453_1_B07. For further details on the construction of this clone see the page at the IMPC portal. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele (Gt(ROSA)26Sortm1(ACTB-cre,-EGFP)Ics). Click here for more information on EUCOMM final vectors. |
| Phenotypic information | Potential phenotyping data in the IMPC portal |
| References | None available |
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 (allele matching)
IMPC phenotypes (gene matching)
- 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
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