- decreased circulating serum albumin level / IMPC
C57BL/6N-Stard7tm1b(EUCOMM)Wtsi/WtsiOulu
Status | Available to order |
EMMA ID | EM:14243 |
International strain name | C57BL/6N-Stard7tm1b(EUCOMM)Wtsi/WtsiOulu |
Alternative name | EPD0176_3_A10 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Stard7tm1b(EUCOMM)Wtsi |
Gene/Transgene symbol | Stard7 |
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 EUCOMM ES clone EPD0176_3_A10. 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 EUCOMM final vectors. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | University of Oulu, Oulu, Finland |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased circulating serum albumin level / IMPC
MGI phenotypes (gene matching)
- dermatitis / MGI
- thick epidermis / MGI
- lung inflammation / MGI
- increased airway responsiveness / MGI
- immune system phenotype / MGI
- respiratory system phenotype / MGI
- hematopoietic system phenotype / MGI
- increased susceptibility to type I hypersensitivity reaction / MGI
- integument phenotype / MGI
- prenatal lethality, incomplete penetrance / MGI
- increased CD11b-high dendritic cell number / MGI
- abnormal respiratory epithelial transmembrane transport / MGI
- abnormal mucous gland morphology / MGI
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