- abnormal motor neuron morphology / MGI
- motor neuron degeneration / MGI
- decreased motor neuron number / MGI
- abnormal neuromuscular synapse morphology / MGI
- hyperresponsive / MGI
- abnormal suckling behavior / MGI
- abnormal posture / MGI
- abnormal vocalization / MGI
- apnea / MGI
- no abnormal phenotype detected / MGI
- abnormal nervous system electrophysiology / MGI
- abnormal axon extension / MGI
- abnormal retinal inner plexiform layer morphology / MGI
- increased motor neuron number / MGI
- neonatal lethality, complete penetrance / MGI
C57BL/6N-Gphnem1(IMPC)Ics/Ics
Status | Available to order |
EMMA ID | EM:15492 |
Citation information | RRID:IMSR_EM:15492 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-Gphnem1(IMPC)Ics/Ics |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Gphnem1(IMPC)Ics |
Gene/Transgene symbol | Gphn |
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 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 | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Hereditary hyperekplexia / Orphanet_3197
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C / Orphanet_308400
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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