- abnormal snout morphology / IMPC
- decreased body length / IMPC
- increased circulating insulin level / IMPC
- decreased erythrocyte cell number / IMPC
- abnormal eyelid aperture / IMPC
- increased circulating creatinine level / IMPC
- increased mean corpuscular hemoglobin / IMPC
- increased blood urea nitrogen level / IMPC
- increased circulating potassium level / IMPC
C57BL/6N-Usp1tm1b(KOMP)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:14404 |
International strain name | C57BL/6N-Usp1tm1b(KOMP)Wtsi/WtsiH |
Alternative name | EPD0039_1_D10 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Usp1tm1b(KOMP)Wtsi |
Gene/Transgene symbol | Usp1 |
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 | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0039_1_D10. 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 using a cell permeable HTN-Cre as described in doi:10.1007/s11248-013-9764-x. Click here for more information on KOMP final vectors. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased circulating potassium level / IMPC
- decreased erythrocyte cell number / IMPC
- abnormal snout morphology / IMPC
- abnormal eyelid aperture / IMPC
- decreased body length / IMPC
- increased mean corpuscular hemoglobin / IMPC
- increased circulating insulin level / IMPC
- increased circulating creatinine level / IMPC
- increased blood urea nitrogen level / IMPC
MGI phenotypes (gene matching)
- delayed bone ossification / MGI
- decreased bone mineral density / MGI
- decreased bone marrow cell number / MGI
- small testis / MGI
- seminiferous tubule degeneration / MGI
- decreased body weight / MGI
- cyanosis / MGI
- increased mortality induced by gamma-irradiation / MGI
- edema / MGI
- reduced female fertility / MGI
- male infertility / MGI
- oligozoospermia / MGI
- decreased circulating alkaline phosphatase level / MGI
- induced chromosome breakage / MGI
- increased bone resorption / MGI
- skeleton phenotype / MGI
- decreased oocyte number / MGI
- abnormal male germ cell morphology / MGI
- abnormal spermatogonia morphology / MGI
- abnormal spermatocyte morphology / MGI
- abnormal spermatid morphology / MGI
- decreased bone volume / MGI
- abnormal osteoid morphology / MGI
- postnatal lethality, incomplete penetrance / MGI
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