Entity Details

Primary name EXOC6B
Entity type gene
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Details

PrimaryID23233
RefseqGeneNG_050967
SymbolEXOC6B
Nameexocyst complex component 6B
Chromosome2
Location2p13.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1999-11-30
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsEXC6B_HUMAN

GO terms

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GOName
GO:0000145 exocyst
GO:0006887 exocytosis
GO:0006893 Golgi to plasma membrane transport
GO:0006904 vesicle docking involved in exocytosis
GO:0015031 protein transport
GO:0016020 membrane

Diseases

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Disease IDSourceNameDescription
618395 OMIMSpondyloepimetaphyseal dysplasia with joint laxity, 3 (SEMDJL3)An autosomal recessive bone disease characterized by multiple joint dislocations at birth, severe joint laxity, scoliosis, gracile metacarpals and metatarsals, delayed bone age and poorly ossified carpal and tarsal bones. The disease may be caused by variants affecting the gene represented in this entry.