C57BL/6N-Sorl1tm1b(EUCOMM)Wtsi/Cnrm
Status | Available to order |
EMMA ID | EM:08449 |
International strain name | C57BL/6N-Sorl1tm1b(EUCOMM)Wtsi/Cnrm |
Alternative name | EPD0532_2_A01 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Sorl1tm1b(EUCOMM)Wtsi |
Gene/Transgene symbol | Sorl1 |
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 | CNR, Consiglio Nazionale delle Ricerche |
Provider affiliation | EMMA-Monterotondo Campus International Development, CNR, Consiglio Nazionale delle Ricerche |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0532_2_A01. 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 (MGI:5285392)). 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 | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Early-onset autosomal dominant Alzheimer disease / Orphanet_1020
IMPC phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal cholinergic neuron morphology / MGI
- abnormal object recognition memory / MGI
- neuron degeneration / MGI
- amyloid beta deposits / MGI
- nervous system phenotype / MGI
- tau protein deposits / MGI
- abnormal vascular wound healing / MGI
- abnormal vascular smooth muscle physiology / MGI
- impaired spatial learning / MGI
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