COX18 Antibody

1. COX20 stabilizes COX2 during insertion of its N-proximal transmembrane domain, and subsequently, COX18 transiently interacts with COX2 to promote translocation across the inner membrane of the COX2 C-tail that contains the apo-CuA site. The release of COX18 from this complex coincides with the binding of the SCO1-SCO2-COA6 copper metallation module to COX2-COX20 to finalize COX2 biogenesis. PMID: 28330871
2. Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) PMID: 20819778
3. Observational study of gene-disease association. (HuGE Navigator) PMID: 20877624
4. Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) PMID: 20379614
5. Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) PMID: 20200953
6. COX18 mutations may be very rare or associated with other phenotypes than isolated COX deficiency in infancy. PMID: 19373256
7. Both hCox18p and hCox19p present significant amino acid identity with the corresponding yeast polypeptides and reveal highly conserved functional domains. PMID: 16212937

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HGNC: 26801

OMIM: 610428

KEGG: hsa:285521

STRING: 9606.ENSP00000295890

UniGene: Hs.356697