- increased circulating alkaline phosphatase level / IMPC
C57BL/6N-Atm1Brd Creb3l1tm1e(EUCOMM)Wtsi/WtsiCnrm
Status | Available to order |
EMMA ID | EM:06200 |
International strain name | C57BL/6N-Atm1Brd Creb3l1tm1e(EUCOMM)Wtsi/WtsiCnrm |
Alternative name | EPD0651_2_E07 |
Strain type | Targeted Mutant Strains : Targeted Non-conditional |
Allele/Transgene symbol | Creb3l1tm1e(EUCOMM)Wtsi |
Gene/Transgene symbol | Creb3l1 |
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 EPD0651_2_E07. For further details on the construction of this clone see the page at the IMPC portal. The targeted allele has lost the 3' loxP site. These mutations cannot be converted into conditional alleles. 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
- Osteogenesis imperfecta type 3 / Orphanet_216812
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased circulating alkaline phosphatase level / IMPC
MGI phenotypes (gene matching)
- fragile skeleton / MGI
- decreased bone mineral density / MGI
- decreased compact bone thickness / MGI
- postnatal growth retardation / MGI
- abnormal bone marrow cell morphology/development / MGI
- abnormal osteoblast morphology / MGI
- abnormal osteoblast differentiation / MGI
- decreased trabecular bone thickness / MGI
- decreased bone ossification / MGI
- decreased bone mineralization / MGI
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