Symbol Name ID |
Rab3gap1
RAB3 GTPase activating protein subunit 1 MGI:2445001 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Spastic diplegia |
Delayed CNS myelination |
Enlarged sylvian cistern |
Perisylvian polymicrogyria |
Agenesis of corpus callosum |
Hypoplasia of the corpus callosum |
Cerebral atrophy |
Cerebellar vermis hypoplasia |
Cerebellar hypoplasia |
Intellectual disability |
Hyperreflexia |
Disease(s) Associated with RAB3GAP1 | ||||||||||||
Warburg micro syndrome 1 |
Mouse Phenotypes | abnormal excitatory postsynaptic currents |
abnormal neurotransmitter secretion |
enhanced paired-pulse facilitation |
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Availability | Mouse Genotype | |||
Rab3gap1tm1Tkss/Rab3gap1tm1Tkss |
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 04/23/2024 MGI 6.23 |
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