- tremors / IMPC
- abnormal femur morphology / IMPC
- abnormal joint morphology / IMPC
- abnormal humerus morphology / IMPC
- abnormal tibia morphology / IMPC
- abnormal auditory brainstem response / IMPC
- abnormal radius morphology / IMPC
- decreased locomotor activity / IMPC
- abnormal ear morphology / IMPC
- decreased prepulse inhibition / IMPC
- abnormal pelvic girdle bone morphology / IMPC
- increased circulating triglyceride level / IMPC
- abnormal ulna morphology / IMPC
- short tibia / IMPC
- increased circulating alkaline phosphatase level / IMPC
C57BL/6N-Col9a2tm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:08189 |
Citation information | RRID:IMSR_EM:08189 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-Col9a2tm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0774_3_F03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Col9a2tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Col9a2 |
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 | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0774_3_F03. 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 | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive Stickler syndrome / Orphanet_250984
- Multiple epiphyseal dysplasia due to collagen 9 anomaly / Orphanet_166002
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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