This gene encodes a protein that is similar to members of the CaiB/baiF CoA-transferase protein family. Mutations in this gene are associated with glutaric aciduria type III. Alternate splicing results in multiple transcript variants.
C7ORF10; chromosome 7 open reading frame 10; caiB/baiF CoA-transferase family protein C7orf10; dermal papilla derived protein 13; DERP13; FLJ11808; ORF19; Russel Silver syndrome candidate; Hypothetical protein LOC79783; Russel-Silver syndrome candidate; Uncharacterized protein C7orf10; dermal papilla-derived protein 13
C7orf10 has several biochemical functions, for example, succinate-hydroxymethylglutarate CoA-transferase activity. Some of the functions are cooperated with other proteins, some of the functions could acted by C7orf10 itself. We selected most functions C7orf10 had, and list some proteins which have the same functions with C7orf10. You can find most of the proteins on our site.
Function succinate-hydroxymethylglutarate CoA-transferase activity
Related Protein C7orf10
C7orf10 Related Articles
Muneta, Y; Kikuma, R; et al. Molecular cloning, chromosomal location, and biological activity of porcine interleukin-21. JOURNAL OF VETERINARY MEDICAL SCIENCE 66:269-275(2004).
Velling, T; Kusche-Gullberg, M; et al. cDNA cloning and chromosomal localization of human alpha(11) integrin - A collagen-binding, I domain-containing, beta(1-)associated integrin alpha-chain present in muscle tissues. JOURNAL OF BIOLOGICAL CHEMISTRY 274:25735-25742(1999).