- decreased circulating phosphate level / IMPC
- persistence of hyaloid vascular system / IMPC
- irregularly shaped pupil / IMPC
- abnormal retina morphology / IMPC
- abnormal locomotor behavior / IMPC
- abnormal placement of pupils / IMPC
- impaired pupillary reflex / IMPC
- abnormal retina blood vessel morphology / IMPC
C57BL/6NTac-Sema3eem1(IMPC)H/H
Status | Available to order |
EMMA ID | EM:13334 |
Citation information | RRID:IMSR_EM:13334 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-Sema3eem1(IMPC)H/H |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Sema3eem1(IMPC)H |
Gene/Transgene symbol | Sema3e |
Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project 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
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- persistence of hyaloid vascular system / IMPC
- irregularly shaped pupil / IMPC
- decreased circulating phosphate level / IMPC
- impaired pupillary reflex / IMPC
- abnormal placement of pupils / IMPC
- abnormal retina blood vessel morphology / IMPC
- abnormal retina morphology / IMPC
- abnormal locomotor behavior / IMPC
MGI phenotypes (gene matching)
- abnormal motor neuron morphology / MGI
- abnormal motor neuron innervation pattern / MGI
- abnormal retina morphology / MGI
- abnormal somite development / MGI
- abnormal retinal vasculature morphology / MGI
- nervous system phenotype / MGI
- behavior/neurological phenotype / MGI
- abnormal intersomitic vessel morphology / MGI
- Bergmeister's papilla / MGI
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