C57BL/6NTac-Fkbp10tm2a(EUCOMM)Wtsi/IcsOrl
Status | Available to order |
EMMA ID | EM:07823 |
Citation information | RRID:IMSR_EM:07823 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/6NTac-Fkbp10tm2a(EUCOMM)Wtsi/IcsOrl |
Alternative name | EPD0142_1_A09 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Fkbp10tm2a(EUCOMM)Wtsi |
Gene/Transgene symbol | Fkbp10 |
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 | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0142_1_A09. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac males, wild-type C57BL/6NTac females |
Stage of embryos | 8-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Bruck syndrome / Orphanet_2771
- Kuskokwim syndrome / Orphanet_1149
- Osteogenesis imperfecta type 3 / Orphanet_216812
- Osteogenesis imperfecta type 4 / Orphanet_216820
IMPC phenotypes (allele matching)
MGI phenotypes (allele matching)
- abnormal cell morphology / MGI
- abnormal craniofacial morphology / MGI
- abnormal forelimb morphology / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal endoplasmic reticulum morphology / MGI
- prenatal growth retardation / MGI
- decreased aorta wall thickness / MGI
- neonatal lethality, complete penetrance / MGI
- abnormal bone collagen fibril morphology / MGI
- abnormal extracellular matrix morphology / MGI
MGI phenotypes (gene matching)
- abnormal cell morphology / MGI
- abnormal craniofacial morphology / MGI
- abnormal forelimb morphology / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal endoplasmic reticulum morphology / MGI
- prenatal growth retardation / MGI
- decreased aorta wall thickness / MGI
- neonatal lethality, complete penetrance / MGI
- abnormal bone collagen fibril morphology / MGI
- abnormal extracellular matrix morphology / MGI
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