- 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 | 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 | C57BL/6N-Tmprss6tm1b(EUCOMM)Wtsi/Ics |
| Alternative name | Tmprss6tm1b(EUCOMM)Wtsi/Ics |
| Strain type | Targeted Mutant Strains : Knock-out |
| 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 | The 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 (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
MGI phenotypes (gene matching)
- decreased hematocrit / MGI
- extramedullary hematopoiesis / MGI
- abnormal hair follicle morphology / MGI
- alopecia / MGI
- sparse hair / MGI
- focal hair loss / MGI
- decreased body size / MGI
- anemia / MGI
- abnormal intestinal mineral absorption / MGI
- postnatal growth retardation / MGI
- abnormal iron level / MGI
- reduced female fertility / MGI
- female infertility / MGI
- abnormal erythrocyte morphology / MGI
- decreased mean corpuscular volume / MGI
- reticulocytosis / MGI
- anisopoikilocytosis / MGI
- microcytic anemia / MGI
- microcytosis / MGI
- decreased hemoglobin content / MGI
- decreased erythrocyte cell number / MGI
- abnormal ovary development / MGI
- pallor / MGI
- maternal effect / MGI
- decreased circulating iron level / MGI
- increased spleen weight / MGI
- hematopoietic system phenotype / MGI
- decreased mean corpuscular hemoglobin / MGI
- abnormal iron homeostasis / MGI
- decreased mean corpuscular hemoglobin concentration / MGI
- decreased liver iron level / MGI
- decreased spleen iron level / MGI
- progressive hair loss / MGI
- increased red blood cell distribution width / MGI
- abnormal hair follicle infundibulum morphology / MGI
- thin hair follicle outer root sheath / MGI
- mortality/aging / MGI
- postnatal lethality, incomplete penetrance / MGI
- increased circulating unsaturated transferrin level / MGI
- decreased pancreas iron level / MGI
- decreased heart iron level / MGI
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