About: SUZ12 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
  • SUZ12 wt Allele
rdfs:subClassOf
OMIM_Number
  • 606245
GenBank_Accession_Number
  • D63881
Semantic_Type
  • Gene or Genome
Preferred_Name
  • SUZ12 wt Allele
UMLS_CUI
  • C2348125
EntrezGene_ID
  • 23512
Legacy_Concept_Name
  • SUZ12_wt_Allele
HGNC_ID
  • HGNC:17101
FULL_SYN
  • Suppressor of Zeste 12 Homolog (Drosophila) wt AlleleSYNCI
  • SUZ12 wt AllelePTNCI
  • CHET9SYNCI
  • JJAZ1SYNCI
  • KIAA0160SYNCI
DEFINITION
  • Human SUZ12 wild-type allele is located in the vicinity of 17q11.2 and is approximately 64 kb in length. This allele, which encodes polycomb protein SUZ12, is involved in the coordination of embryonic development and the mediation of histone methylation. A chromosomal aberration involving this gene, translocation t(7;17)(p15;q21) with the JAZF1 gene, is associated with endometrial stromal tumors.NCISwissProt
DesignNote
  • The translocation of the JAZF1-SUZ12 genes generates a gene product consisting of the N-terminus part of JAZF1 and the C-terminus part of SUZ12. (SwissProt)
code
  • C73546
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