Symbol Name ID |
Megf10
multiple EGF-like-domains 10 MGI:2685177 |
Darker colors indicate more annotations |
Human Phenotypes | Facial palsy |
Tongue fasciculations |
Dysphagia |
Difficulty walking |
Diaphragmatic paralysis |
Abnormal motor nerve conduction velocity |
Intellectual disability |
Areflexia |
Hyporeflexia |
Motor delay |
Seizure |
Disease(s) Associated with MEGF10 | |||||||||||
congenital myopathy 10B | |||||||||||
early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome |
Mouse Phenotypes | increased hindbrain apoptosis |
abnormal cerebellum morphology |
abnormal amacrine cell morphology |
abnormal retina horizontal cell morphology |
abnormal astrocyte physiology |
|
Availability | Mouse Genotype | |||||
Megf10tm1(KOMP)Vlcg/Megf10tm1(KOMP)Vlcg | ||||||
Megf10tm1a(KOMP)Jrs/Megf10tm1a(KOMP)Jrs | ||||||
Megf10tm1(KOMP)Vlcg/Megf10+ | ||||||
Megf10tm1a(KOMP)Jrs/Megf10+ |
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 08/02/2024 MGI 6.24 |
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