EXOC6B Chromosome 2

Exocyst complex component 6B
13 variants 13 Health Risk

Upload your DNA to see your personal genotypes for variants in EXOC6B.

What This Gene Does
This gene encodes a protein which is a part of the evolutionarily conserved exocyst, a multimeric protein complex necessary for exocytosis, which in turn, is crucial for cell growth, polarity and migration. Disruption of this gene may be associated with phenotypes exhibiting multiple symptoms including intellectual disability and developmental delay (DD). [provided by RefSeq, Jun 2016]
Gene Info
Gene Group
Exocyst complex
Locus Type
gene with protein product
Location
2p13.2
Ensembl
ENSG00000144036
Associated Conditions (2)
Spondyloepimetaphyseal dysplasia with joint laxity
type 3
Key Variants
All Variants (13)
RSID Category Clinical Significance Conditions
RS1553417206 Health Risk Conflicting classifications of pathogenicity
RS200227562 Health Risk Conflicting classifications of pathogenicity
RS2105685436 Health Risk Conflicting classifications of pathogenicity
RS773011698 Health Risk Conflicting classifications of pathogenicity
RS1064795104 Health Risk Likely pathogenic
RS2105672766 Health Risk Likely pathogenic
RS2466370942 Health Risk Likely pathogenic
RS2467829039 Health Risk Likely pathogenic Spondyloepimetaphyseal dysplasia with joint laxity, type 3, Spondyloepimetaphyseal dysplasia with joint laxity
RS374381770 Health Risk Likely pathogenic
RS1294100541 Health Risk Pathogenic Spondyloepimetaphyseal dysplasia with joint laxity, type 3, Spondyloepimetaphyseal dysplasia with joint laxity
RS2104774484 Health Risk Pathogenic Spondyloepimetaphyseal dysplasia with joint laxity, type 3, Spondyloepimetaphyseal dysplasia with joint laxity
RS2467737048 Health Risk Pathogenic
RS1195320854 Health Risk Pathogenic/Likely pathogenic
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