Symbol Name ID |
Agrn
agrin MGI:87961 |
* | Aspects of the system are reported to show a normal phenotype. |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Easy fatigability |
Disease(s) Associated with AGRN | |
congenital myasthenic syndrome 8 |
Mouse Phenotypes | nervous system phenotype |
abnormal innervation |
abnormal innervation pattern to muscle |
decreased CNS synapse formation |
abnormal axon morphology |
abnormal neuromuscular synapse morphology |
failure of neuromuscular synapse presynaptic differentiation |
increased post-tetanic potentiation |
abnormal paired-pulse inhibition |
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Availability | Mouse Genotype | |||||||||
AgrnGt(Ex192)Byg/AgrnGt(Ex192)Byg | ||||||||||
Agrnnmf380/Agrnnmf380 | * | ! | ||||||||
Agrntm1Jrs/Agrntm1Jrs | * | |||||||||
Agrntm3Jrs/Agrntm3Jrs | ||||||||||
Agrntm4Jrs/Agrntm4Jrs | ||||||||||
Agrntm5Jrs/Agrntm5Jrs | * | |||||||||
Agrntm1Rwb/Agrntm1Rwb Tg(Pax3-cre)1Joe/0 (conditional) |
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Agrntm1Rwb/Agrntm1Rwb Tg(Tek-cre)1Ywa/? (conditional) |
* |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 05/28/2024 MGI 6.13 |
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