archain 1 | |||||||
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Identifiers | |||||||
Symbol | ARCN1 | ||||||
Alt. symbols | COPD | ||||||
NCBI gene | 372 | ||||||
HGNC | 649 | ||||||
OMIM | 600820 | ||||||
RefSeq | NM_001655 | ||||||
UniProt | P48444 | ||||||
Other data | |||||||
Locus | Chr. 11 q23.3 | ||||||
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Archain is a human protein that is encoded by gene which is located on chromosome 11. Also known as ARCN1, it plays a role in eukaryotic cell biology.
It is part of the COPI coatomer complex.
References
- Xu X, Kedlaya R, Higuchi H, et al. (2010). "Mutation in archain 1, a subunit of COPI coatomer complex, causes diluted coat color and Purkinje cell degeneration". PLOS Genet. 6 (5): e1000956. doi:10.1371/journal.pgen.1000956. PMC 2873907. PMID 20502676.
External links
- Archain at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
Membrane protein: vesicular transport proteins (TC 1F) | |||||||||||||||||||||||||||
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Synaptic vesicle |
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COPI | |||||||||||||||||||||||||||
COPII | |||||||||||||||||||||||||||
RME/Clathrin | |||||||||||||||||||||||||||
Caveolae | |||||||||||||||||||||||||||
Other/ungrouped |
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See also vesicular transport protein disorders |
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