About: RNF213 wt Allele     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz:8890 associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • RNF213 wt Allele
rdfs:subClassOf
OMIM_Number
  • 613768
GenBank_Accession_Number
  • AK074030
Semantic_Type
  • Gene or Genome
Preferred_Name
  • RNF213 wt Allele
NCI_META_CUI
  • CL429843
EntrezGene_ID
  • 57674
HGNC_ID
  • HGNC:14539
FULL_SYN
  • hCG_1812857SYNCI
  • Ring Finger Protein 213 wt AlleleSYNCI
  • DKFZp762N1115SYNCI
  • RNF213 wt AllelePTNCI
  • ALO17SYNCI
  • NET57SYNCI
  • MGC9929SYNCI
  • ALK Lymphoma Oligomerization Partner on Chromosome 17 GeneSYNCI
  • Chromosome 17 Open Reading Frame 27 GeneSYNCI
  • FLJ13051SYNCI
  • MGC46622SYNCI
  • KIAA1554SYNCI
  • KIAA1618SYNCI
  • C17orf27SYNCI
DEFINITION
  • Human RNF213 wild-type allele is located in the vicinity of 17q25.3 and is approximately 135 kb in length. This allele, which encodes RING finger protein 213, may play a role in the regulation of protein ubiquitination. A chromosomal translocation t(2;17)(p23;q25) of this gene with the ALK gene is associated with anaplastic large cell lymphoma.NCI
DesignNote
  • The RNF213 gene also encodes protein ALO17. (EntrezGene)
code
  • C97391
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