EXOC6

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Exocyst complex component 6 is a protein that in humans is encoded by the EXOC6 gene.[5]

AliasesEXOC6, EXOC6A, SEC15, SEC15L, SEC15L1, SEC15L3, Sec15p, exocyst complex component 6
End93,059,493 bp[1]
Quick facts Identifiers, Aliases ...
EXOC6
Identifiers
AliasesEXOC6, EXOC6A, SEC15, SEC15L, SEC15L1, SEC15L3, Sec15p, exocyst complex component 6
External IDsOMIM: 609672; MGI: 1351611; HomoloGene: 41305; GeneCards: EXOC6; OMA:EXOC6 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001013848
NM_019053
NM_001319194
NM_001319195
NM_001319200

NM_175353

RefSeq (protein)

NP_001013870
NP_001306123
NP_001306124
NP_001306129
NP_061926

n/a

Location (UCSC)Chr 10: 92.83 – 93.06 MbChr 19: 37.51 – 37.67 Mb
PubMed search[3][4]
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Function

The protein encoded by this gene is highly similar to the Saccharomyces cerevisiae SEC15 gene product, which is essential for vesicular traffic from the Golgi apparatus to the cell surface in yeast. It is one of the components of a multiprotein complex required for exocytosis. The 5' portion of this gene and two neighboring cytochrome p450 genes are included in a deletion that results in an autosomal dominant form of nonsyndromic optic nerve aplasia (ONA). Alternative splicing and the use of alternative promoters results in multiple transcript variants. A paralogous gene encoding a similar protein is present on chromosome 2.

References

Further reading

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