C57BL/6N-Cbx2tm1a(KOMP)Wtsi/H
Status | Available to order |
EMMA ID | EM:05905 |
International strain name | C57BL/6N-Cbx2tm1a(KOMP)Wtsi/H |
Alternative name | EPD0379_3_F12 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cbx2tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Cbx2 |
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 KOMP ES clone EPD0379_3_F12. 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
- 46,XY complete gonadal dysgenesis / Orphanet_242
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- malocclusion / MGI
- abnormal scapula morphology / MGI
- abnormal colon morphology / MGI
- small ovary / MGI
- abnormal body weight / MGI
- arrested T cell differentiation / MGI
- secondary sex reversal / MGI
- premature death / MGI
- abnormal primary sex determination / MGI
- abnormal secondary sex determination / MGI
- true hermaphroditism / MGI
- vertebral transformation / MGI
- decreased rib number / MGI
- abnormal cervical atlas morphology / MGI
- abnormal skeleton morphology / MGI
- agonadal / MGI
- decreased splenocyte proliferation / MGI
- fusion of atlas and occipital bones / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- decreased fibroblast proliferation / MGI
- decreased sternebra number / MGI
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