C57BL/6N-Ctc1tm1a(KOMP)Wtsi/Ieg
Status | Available to order |
EMMA ID | EM:10068 |
International strain name | C57BL/6N-Ctc1tm1a(KOMP)Wtsi/Ieg |
Alternative name | EPD0302_2_B12 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Ctc1tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Ctc1 |
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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | This mouse line originates from KOMP ES clone EPD0302_2_B12. 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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6NTac |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Dyskeratosis congenita / Orphanet_1775
- Coats plus syndrome / Orphanet_313838
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- decreased cell proliferation / MGI
- sparse hair / MGI
- small spleen / MGI
- small thymus / MGI
- decreased body size / MGI
- impaired hematopoiesis / MGI
- premature death / MGI
- abnormal bone marrow cell morphology/development / MGI
- no phenotypic analysis / MGI
- abnormal telomere length / MGI
- abnormal hematopoietic stem cell morphology / MGI
- decreased hematopoietic stem cell number / MGI
- early cellular replicative senescence / MGI
- abnormal DNA repair / MGI
- chromosomal instability / MGI
- decreased splenocyte proliferation / MGI
- decreased fibroblast proliferation / MGI
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