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

AttributesValues
rdf:type
rdfs:label
  • Imprinting Gene
rdfs:subClassOf
Semantic_Type
  • Gene or Genome
Preferred_Name
  • Imprinting Gene
UMLS_CUI
  • C1708477
Legacy_Concept_Name
  • Imprinting_Gene
FULL_SYN
  • Imprinting GenePTNCI
DEFINITION
  • A gene that does not exhibit equal expression of both alleles due to repression or inactivation, resulting in the genetic non-equivalence of mammalian paternal and maternal genomes.NCI
DesignNote
  • Several severe human genetic disorders are associated with imprinted genes such as Beckwith-Wiedemann, Prader-Willi and Angelman syndromes.
code
  • C54401
is rdfs:subClassOf of
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