- 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
C57BL/6N-Atm1Brd Tmprss6tm1a(EUCOMM)Wtsi/Ics
Status | Available to order |
EMMA ID | EM:10677 |
International strain name | C57BL/6N-Atm1Brd Tmprss6tm1a(EUCOMM)Wtsi/Ics |
Alternative name | EPD0453_1_B07 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Tmprss6tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Tmprss6 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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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. |
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 |
Animals used for archiving | heterozygous C57BL/6N |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- IRIDA syndrome / Orphanet_209981
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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