- 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 |
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 |
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
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