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C9ORF100

  • Official Full Name

    chromosome 9 open reading frame 100

  • Synonyms

    C9ORF100; chromosome 9 open reading frame 100; vav-like protein C9orf100; FLJ14642; Hypothetical protein LOC84904; MGC44886; RP11 331F9.7; Vav like protein C9orf100; RP11-331F9.7;
Species Cat.# Product name Source (Host) Tag Protein Length Price
Human C9orf100-10593H Recombinant Human C9orf100, His-tagged E.coli His 1-335a.a.
Human C9orf100-7944HCL Recombinant Human C9orf100 293 Cell Lysate HEK293 N/A
  • Involved Pathway
  • Protein Function
  • Interacting Protein
  • C9ORF100 Related Articles

C9ORF100 involved in several pathways and played different roles in them. We selected most pathways C9ORF100 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with C9ORF100 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

Pathway Name Pathway Related Protein

C9ORF100 has several biochemical functions, for example, Rho guanyl-nucleotide exchange factor activity, protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by C9ORF100 itself. We selected most functions C9ORF100 had, and list some proteins which have the same functions with C9ORF100. You can find most of the proteins on our site.

Function Related Protein
Rho guanyl-nucleotide exchange factor activityARHGEF33;BCR;FGD4;VAV3;ITSN2;ARHGEF17;ARHGEF7A;ARHGEF10;PLEKHG4
protein bindingEFEMP2;ETNK1;LTBR;KIF4A;NVL;OBFC1;ANKS4B;IGSF1;CARD11

C9ORF100 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 C9ORF100 here. Most of them are supplied by our site. Hope this information will be useful for your research of C9ORF100.

CALCOCO2; TIFA; DVL2; RBPMS

Yamakawa, M; Ito, D; et al. Characterization of the dipeptide repeat protein in the molecular pathogenesis of c9FTD/ALS. HUMAN MOLECULAR GENETICS 24:1630-1645(2015).
Geevasinga, N; Menon, P; et al. Axonal Ion Channel Dysfunction in C9orf72 Familial Amyotrophic Lateral Sclerosis. JAMA NEUROLOGY 72:49-57(2015).
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