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Symbol
Name
ID

Megf10
multiple EGF-like-domains 10
MGI:2685177

Phenotype annotations related to nervous system

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	Facial palsy	Tongue fasciculations	Dysphagia	Difficulty walking	Diaphragmatic paralysis	Abnormal motor nerve conduction velocity	Intellectual disability	Areflexia	Hyporeflexia	Motor delay	Seizure
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	increased hindbrain apoptosis	abnormal cerebellum morphology	abnormal amacrine cell morphology	abnormal retina horizontal cell morphology	abnormal astrocyte physiology
	Megf10^{tm1(KOMP)Vlcg}/Megf10^{tm1(KOMP)Vlcg}
	Megf10^{tm1a(KOMP)Jrs}/Megf10^{tm1a(KOMP)Jrs}
	Megf10^{tm1(KOMP)Vlcg}/Megf10⁺
	Megf10^{tm1a(KOMP)Jrs}/Megf10⁺

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 08/02/2024 MGI 6.24