C57BL/6N-Crb2tm1c(KOMP)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:11129 |
Citation information | RRID:IMSR_EM:11129 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-Crb2tm1c(KOMP)Wtsi/WtsiH |
Alternative name | EPD0603_1_B06 |
Strain type | Targeted Mutant Strains : Targeted Conditional |
Allele/Transgene symbol | Crb2tm1c(KOMP)Wtsi |
Gene/Transgene symbol | Crb2 |
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 line originates from KOMP ES clone EPD0603_1_B06, after breeding with a Flp recombinase deleter line to convert the original targeted allele tm1a (knock-out first allele) into a conditional allele tm1c. 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 |
Animals used for archiving | heterozygous C57BL/6NTac (USA) males |
Breeding at archiving centre | C57BL/6NTac background |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Genetic steroid-resistant nephrotic syndrome / Orphanet_656
- Ventriculomegaly-cystic kidney disease / Orphanet_443988
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal foregut morphology / MGI
- open neural tube / MGI
- abnormal mesoderm development / MGI
- abnormal endoderm development / MGI
- abnormal somite development / MGI
- abnormal gastrulation / MGI
- increased embryo size / MGI
- abnormal embryonic tissue morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal primitive streak morphology / MGI
- abnormal chorioallantoic fusion / MGI
- abnormal notochord morphology / MGI
- abnormal digestive system development / MGI
- abnormal vitelline vasculature morphology / MGI
- abnormal embryonic epiblast morphology / MGI
- failure of initiation of embryo turning / MGI
- abnormal embryonic neuroepithelium morphology / MGI
- small allantois / MGI
- failure of chorioallantoic fusion / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal visceral yolk sac blood island morphology / MGI
- abnormal head fold morphology / MGI
- absent heart tube / MGI
- small amniotic cavity / MGI
- abnormal anterior primitive streak morphology / MGI
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