- 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 |
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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