C3ORF58 Protein, chromosome 3 open reading frame 58

C3ORF58

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C3ORF58

Official Full Name chromosome 3 open reading frame 58
Synonyms C3ORF58; chromosome 3 open reading frame 58; UPF0672 protein C3orf58; MGC33365; DIA1; Golgi protein GoPro49
    • Species :
    • Human
    • Source :
    • E.coli
    • Wheat Germ
    • Tag :
    • GST
    • His
    Species Cat.# Product name Source (Host) Tag Protein Length Price
    Human C3orf58-0042H Recombinant Human C3orf58 Protein, GST-Tagged Wheat Germ GST
    Human C3orf58-1825H Recombinant Human C3orf58 Protein, His-tagged E.coli His

    C3ORF58 involved in several pathways and played different roles in them. We selected most pathways C3ORF58 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with C3ORF58 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

    Pathway Name Pathway Related Protein

    C3ORF58 has several biochemical functions, for example, . Some of the functions are cooperated with other proteins, some of the functions could acted by C3ORF58 itself. We selected most functions C3ORF58 had, and list some proteins which have the same functions with C3ORF58. You can find most of the proteins on our site.

    Function Related Protein

    C3ORF58 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with C3ORF58 here. Most of them are supplied by our site. Hope this information will be useful for your research of C3ORF58.

    van Blitterswijk, M; Dejesus-Hernandez, M; et al. Association between repeat sizes and clinical and pathological characteristics in carriers of C90RF72 repeat expansions (Xpansize-72): a cross-sectional cohort study. LANCET NEUROLOGY 12:978-988(2013).
    Thi, HTT; Zhang, ZJ; et al. Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28. JOURNAL OF HUMAN GENETICS 58:33-39(2013).

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