About Help FAQ

Symbol
Name
ID

Rab18
RAB18, member RAS oncogene family
MGI:102790

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Microcephaly

Secondary microcephaly

Ankle clonus

Lower limb spasticity

Spastic tetraplegia

Ventriculomegaly

Polymicrogyria

Cerebral cortical atrophy

Hypoplasia of the corpus callosum

Absent speech

Intellectual disability, profound

Primitive reflex

Inability to walk

Global developmental delay

Bilateral tonic-clonic seizure

Myoclonic seizure

Disease(s) Associated with RAB18

Warburg micro syndrome 3

Mouse Phenotypes		abnormal nervous system morphology	abnormal corpus callosum morphology	abnormal neuromuscular synapse morphology	optic nerve degeneration	abnormal dorsal spinal root morphology	abnormal sciatic nerve morphology	axon degeneration
Availability	Mouse Genotype	abnormal nervous system morphology	abnormal corpus callosum morphology	abnormal neuromuscular synapse morphology	optic nerve degeneration	abnormal dorsal spinal root morphology	abnormal sciatic nerve morphology	axon degeneration
	Rab18^{Gt(EUCE0233a03)Hmgu}/Rab18^{Gt(EUCE0233a03)Hmgu}
	Rab18^m1Hongc/Rab18^m1Hongc

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 04/23/2024 MGI 6.23