- 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 |
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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