- abnormal nail morphology / IMPC
- tremors / IMPC
- cataract / IMPC
- abnormal gait / IMPC
- decreased exploration in new environment / IMPC
- increased startle reflex / IMPC
- limb grasping / IMPC
- iris synechia / IMPC
- decreased circulating serum albumin level / IMPC
- decreased circulating total protein level / IMPC
- increased circulating iron level / IMPC
- preweaning lethality, incomplete penetrance / IMPC
C57BL/6N-Sema3ftm1b(EUCOMM)Hmgu/H
| Status | Only small colony available |
| EMMA ID | EM:16270 |
| Citation information | RRID:IMSR_EM:16270 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-Sema3ftm1b(EUCOMM)Hmgu/H |
| Alternative name | HEPD0570_6_A04 |
| Strain type | Targeted Mutant Strains |
| Allele/Transgene symbol | Sema3ftm1b(EUCOMM)Hmgu |
| Gene/Transgene symbol | Sema3f |
| 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 | Mary Lyon Centre at MRC Harwell |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | This mouse line originates from EUCOMM ES clone HEPD0570_6_A04. For further details on the construction of this clone see the page at the IMPC portal. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele. Click here for more information on EUCOMM final vectors. |
| 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)
- abnormal nail morphology / IMPC
- tremors / IMPC
- increased startle reflex / IMPC
- iris synechia / IMPC
- decreased exploration in new environment / IMPC
- limb grasping / IMPC
- abnormal gait / IMPC
- decreased circulating total protein level / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- cataract / IMPC
- increased circulating iron level / IMPC
- decreased circulating serum albumin level / IMPC
MGI phenotypes (gene matching)
- abnormal nervous system tract morphology / MGI
- abnormal hippocampus development / MGI
- abnormal oculomotor nerve morphology / MGI
- absent trochlear nerve / MGI
- decreased body size / MGI
- abnormal lymphatic vessel morphology / MGI
- abnormal innervation / MGI
- abnormal axon guidance / MGI
- abnormal nervous system development / MGI
- abnormal habenula morphology / MGI
- abnormal neuronal migration / MGI
- abnormal anterior commissure morphology / MGI
- abnormal axon fasciculation / MGI
- abnormal lymphatic vessel endothelial cell morphology / MGI
- abnormal lymphatic system physiology / MGI
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