Entity Details

Primary name RHOBTB2
Entity type gene
Source Source Link

Details

PrimaryID23221
RefseqGeneNG_047133
SymbolRHOBTB2
NameRho related BTB domain containing 2
Chromosome8
Location8p21.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-05-18
ModificationDate2021-06-22

Ontological Relatives

UniProt IDsRHBT2_HUMAN

GO terms

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GOName
GO:0003924 GTPase activity
GO:0005525 GTP binding
GO:0005856 cytoskeleton
GO:0005886 plasma membrane
GO:0005938 cell cortex
GO:0007015 actin filament organization
GO:0007163 establishment or maintenance of cell polarity
GO:0007264 small GTPase mediated signal transduction
GO:0008360 regulation of cell shape
GO:0010008 endosome membrane
GO:0019901 protein kinase binding
GO:0030865 cortical cytoskeleton organization
GO:0031410 cytoplasmic vesicle
GO:0032956 regulation of actin cytoskeleton organization
GO:0042995 cell projection
GO:0043231 intracellular membrane-bounded organelle
GO:0043652 engulfment of apoptotic cell

Diseases

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Disease IDSourceNameDescription
618004 OMIMDevelopmental and epileptic encephalopathy 64 (DEE64)A form of epileptic encephalopathy, a heterogeneous group of severe childhood onset epilepsies characterized by refractory seizures, neurodevelopmental impairment, and poor prognosis. Development is normal prior to seizure onset, after which cognitive and motor delays become apparent. DEE64 is an autosomal dominant form characterized by onset of seizures usually in the first year of life. Seizure types are variable and include focal dyscognitive and generalized tonic-clonic seizures, as well as febrile seizures in the mildest affected individuals. Seizures tend to respond to medical treatment. The disease is caused by variants affecting the gene represented in this entry.