About: UBQLN2 wt Allele     Goto   Sponge   NotDistinct   Permalink

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

AttributesValues
rdf:type
rdfs:label
  • UBQLN2 wt Allele
rdfs:subClassOf
OMIM_Number
  • 300264
GenBank_Accession_Number
  • AF189009
Semantic_Type
  • Gene or Genome
Preferred_Name
  • UBQLN2 wt Allele
NCI_META_CUI
  • CL435682
EntrezGene_ID
  • 29978
HGNC_ID
  • HGNC:12509
FULL_SYN
  • DSK2SYNCI
  • UBQLN2 wt AllelePTNCI
  • Dsk2SYNCI
  • Ubiquilin 2 wt Allele Chap1SYNCI
  • LIC-2SYNCI
  • ALS15SYNCI
  • N4BP4SYNCI
  • CHAP1SYNCI
  • PLIC2SYNCI
  • NEDD4 Binding Protein 4 GeneSYNCI
  • PLIC-2SYNCI
  • RIHFB2157SYNCI
  • HRIHFB2157SYNCI
  • CHAP1/DSK2SYNCI
  • Ubiquilin 2 wt AlleleSYNCI
DEFINITION
  • Human UBQLN2 wild-type allele is located in the vicinity of Xp11.21 and is approximately 3 kb in length. This allele, which encodes ubiquilin-2 protein, may be involved in the regulation of proteasome activity. Mutation of the gene is associated with amyotrophic lateral sclerosis type 15.NCI
code
  • C101350
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