- abnormal coat/hair pigmentation / IMPC
- increased lactate dehydrogenase level / IMPC
- abnormal incisor color / IMPC
- abnormal humerus morphology / IMPC
- decreased body weight / IMPC
- increased circulating creatine kinase level / IMPC
- abnormal lens morphology / IMPC
- decreased bone mineral density / IMPC
- decreased body length / IMPC
- cataract / IMPC
- abnormal tibia morphology / IMPC
- abnormal eye morphology / IMPC
- abnormal tooth morphology / IMPC
- decreased bone mineral content / IMPC
- increased circulating alanine transaminase level / IMPC
- increased circulating calcium level / IMPC
- abnormal coat/ hair morphology / IMPC
C57BL/6-Sparctm1c(EUCOMM)Wtsi/Orl
Status | Available to order |
EMMA ID | EM:14932 |
Citation information | RRID:IMSR_EM:14932 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | C57BL/6-Sparctm1c(EUCOMM)Wtsi/Orl |
Alternative name | Sparc-tm1c |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Sparctm1c(EUCOMM)Wtsi |
Gene/Transgene symbol | Sparc |
Information from provider
Provider | Cécile FREMOND |
Provider affiliation | CNRS-TAAM-CDTA-UAR44 |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0060_1_A07. For further details on the construction of this clone see the relevant page at the IMPC portal (https://www.mousephenotype.org/data/alleles/MGI:98373/tm1a(EUCOMM)Wtsi). Rederived tm1a mice (EMMA strain EM:05296) have been crossed with flp recombinase-deleter mice (EMMA strain EM:05490, C57BL/6NTac-Gt(ROSA)26Sortm2(CAG-flpo,-EYFP)Ics/Ics) to obtain the tm1c allele. |
Phenotypic information | Homozygous:Homozygous mice have not been generated.Heterozygous:Nothing |
Breeding history | Rederived tm1a mice (EMMA strain EM:05296) have been crossed with flp-deleter mice EMMA strain EM:05490) to obtain the tm1c allele. |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous B6Brd;B6N-Tyrc-Brd males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Osteogenesis imperfecta type 4 / Orphanet_216820
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- decreased bone mineral density / MGI
- abnormal trabecular bone morphology / MGI
- abnormal tibia morphology / MGI
- decreased body weight / MGI
- abnormal lens morphology / MGI
- cataract / MGI
- retinal degeneration / MGI
- hypoactivity / MGI
- abnormal skeleton physiology / MGI
- abnormal bone strength / MGI
- eye inflammation / MGI
- abnormal coat/hair pigmentation / MGI
- abnormal eye morphology / MGI
- abnormal tooth morphology / MGI
- enhanced wound healing / MGI
- abnormal lens fiber morphology / MGI
- delayed wound healing / MGI
- abnormal bone remodeling / MGI
- retinal detachment / MGI
- abnormal lens capsule morphology / MGI
- abnormal lens epithelium morphology / MGI
- increased tumor growth/size / MGI
- abnormal retinal layer morphology / MGI
- abnormal osteoclast morphology / MGI
- decreased osteoclast cell number / MGI
- abnormal osteoblast morphology / MGI
- decreased osteoblast cell number / MGI
- abnormal humerus morphology / MGI
- hematopoietic system phenotype / MGI
- abnormal skeleton morphology / MGI
- decreased mean corpuscular hemoglobin concentration / MGI
- vitreous body inflammation / MGI
- ruptured lens capsule / MGI
- abnormal incisor color / MGI
- subcapsular cataracts / MGI
- posterior subcapsular cataracts / MGI
- cortical cataracts / MGI
Information on how we integrate external resources can be found here
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