C57BL/6N-Atm1Brd Gpc6tm2a(EUCOMM)Wtsi/WtsiBiat
Status | Available to order |
EMMA ID | EM:06012 |
Citation information | RRID:IMSR_EM:06012 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/6N-Atm1Brd Gpc6tm2a(EUCOMM)Wtsi/WtsiBiat |
Alternative name | EPD0547_5_C04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Gpc6tm2a(EUCOMM)Wtsi |
Gene/Transgene symbol | Gpc6 |
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 EPD0547_5_C04. 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 | University of Veterinary Medicine, Vienna, Austria |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive omodysplasia / Orphanet_93329
IMPC phenotypes (allele matching)
MGI phenotypes (gene matching)
- cleft palate / MGI
- short tibia / MGI
- short fibula / MGI
- short femur / MGI
- abnormal long bone epiphyseal plate proliferative zone / MGI
- abnormal long bone diaphysis morphology / MGI
- decreased length of long bones / MGI
- absent nasal septum / MGI
- small cranium / MGI
- decreased fetal weight / MGI
- neonatal lethality, complete penetrance / MGI
- decreased chondrocyte proliferation / MGI
- small snout / MGI
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