C57BL/6NTac-Ift122tm1a(EUCOMM)Wtsi/IcsOrl
Status | Available to order |
EMMA ID | EM:07822 |
Citation information | RRID:IMSR_EM:07822 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/6NTac-Ift122tm1a(EUCOMM)Wtsi/IcsOrl |
Alternative name | EPD0155_2_E05 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Ift122tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Ift122 |
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 | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0155_2_E05. 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 | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac males, wild-type C57BL/6NTac females |
Stage of embryos | 8-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Cranioectodermal dysplasia / Orphanet_1515
IMPC phenotypes (allele matching)
MGI phenotypes (gene matching)
- enlarged heart / MGI
- abnormal cell morphology / MGI
- abnormal head morphology / MGI
- polydactyly / MGI
- exencephaly / MGI
- open neural tube / MGI
- abnormal spinal cord morphology / MGI
- abnormal eye development / MGI
- abnormal left-right axis patterning / MGI
- hemorrhage / MGI
- abnormal eye morphology / MGI
- abnormal neural tube morphology / MGI
- situs inversus / MGI
- abnormal abdominal wall morphology / MGI
- abnormal cell cycle checkpoint function / MGI
- polysyndactyly / MGI
- abnormal spinal cord interneuron morphology / MGI
- abnormal motile primary cilium morphology / MGI
- absent embryonic cilia / MGI
- delayed embryo turning / MGI
- abnormal direction of heart looping / MGI
- increased motor neuron number / MGI
- ectrodactyly / MGI
- abnormal limb development / MGI
- decreased physiological sensitivity to xenobiotic / MGI
- decreased sensitivity to induced cell death / MGI
- preaxial polydactyly / MGI
- abnormal pharyngeal arch development / MGI
- right-sided stomach / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- decreased embryonic cilium length / MGI
- delayed limb development / MGI
- elongated neck / MGI
- enlarged pharyngeal arch / MGI
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