- 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 |
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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