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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	Cat.#	Product name	Source (Host)	Tag	Protein Length	Price
Human	C3orf58-0042H	Recombinant Human C3orf58 Protein, GST-Tagged	Wheat Germ	GST		Inquiry
Human	C3orf58-2603HF	Recombinant Full Length Human C3orf58 Protein, GST-tagged	In Vitro Cell Free System	GST	430 amino acids	Inquiry
Human	C3orf58-1825H	Recombinant Human C3orf58 Protein, His-tagged	E.coli	His		Inquiry

C3ORF58 Related Articles

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).