• Official Full Name
  • ring finger protein 213
  • Background
  • Ring finger protein 213 is a protein that in humans is encoded by the RNF213 gene.
  • Synonyms
  • RNF213; ring finger protein 213; C17orf27, chromosome 17 open reading frame 27 , KIAA1618 , moyamoya disease 2 , Moyamoya disease 2 , MYMY2; KIAA1554; NET57; mysterin; ALK lymphoma oligomerization partner on chromosome 17; ALO
Source (Host):HEK293Species:Human
Product nameRecombinant Human RNF213 Protein, MYC/DDK-tagged
Source (Host):HEK293Species:Human
Product nameRecombinant Human RNF213 lysate

Protein Function

RNF213 has several biochemical functions, for example, ATPase activity, ligase activity, protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by RNF213 itself. We selected most functions RNF213 had, and list some proteins which have the same functions with RNF213. You can find most of the proteins on our site.
Related Protein
Function ATPase activity
Related Protein HSPA8; ABCG4B; KIFC3; ATAD2; HAND2; EIF4A2; ABCB3L1; KIF22; ATAD2B; ABCA4
Function ligase activity
Related Protein UBE2I; ADSSL; LIG4; NEDD4; G2E3; UBE2G1B; UBR5; RAD18; UBR3; LIPT2
Function protein binding
Related Protein GH1; RPS25; LDHB; EIF4E2; FCGR2B; ERLEC1; DOHH; C19orf46; TAF9; COX4I1
Function ubiquitin-protein transferase activity
Related Protein NLRC4; RNF144B; ARIH1L; MIB2; FBXO25; CDC23; RNF144AA; ZNRF1; RNF43; SHPRH
Function zinc ion binding
Related Protein DUSP12; RNF139; CA5A; TRIM30A; KAT7B; ZDHHC23B; ZNF385D; MTF2; NRAP; ZEB1

Interacting Protein

RNF213 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 RNF213 here. Most of them are supplied by our site. Hope this information will be useful for your research of RNF213.
vpu; HLA-C; MCRS1; PLAC9; PTPN1; Kif4; Ube2k; CBX2; RNASEH2B; Rpl35; MRPL50

RNF213 Related Articles

Cecchi, AC; Guo, DC; et al. RNF213 Rare Variants in an Ethnically Diverse Population With Moyamoya Disease. STROKE 45:3200-3207(2014).
Macedo, DB; Abreu, AP; et al. Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM 99:E1097-E1103(2014).