C57BL/6N-Atm1Brd Crb2tm1a(KOMP)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:07854 |
Citation information | RRID:IMSR_EM:07854 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-Atm1Brd Crb2tm1a(KOMP)Wtsi/WtsiH |
Alternative name | EPD0603_1_B06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Crb2tm1a(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 mouse line originates from KOMP ES clone EPD0603_1_B06. 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
- Genetic steroid-resistant nephrotic syndrome / Orphanet_656
- Ventriculomegaly-cystic kidney disease / Orphanet_443988
IMPC phenotypes (allele 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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