About: CHD2 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
  • CHD2 wt Allele
rdfs:subClassOf
OMIM_Number
  • 602119
GenBank_Accession_Number
  • AF006514
Semantic_Type
  • Gene or Genome
Preferred_Name
  • CHD2 wt Allele
UMLS_CUI
  • C2698724
EntrezGene_ID
  • 1106
Legacy_Concept_Name
  • CHD2_wt_Allele
HGNC_ID
  • HGNC:1917
FULL_SYN
  • Chromodomain Helicase DNA Binding Protein 2 wt AlleleSYNCI
  • DKFZp547I1315SYNCI
  • DKFZp781D1727SYNCI
  • DKFZp686E01200SYNCI
  • CHD2 wt AllelePTNCI
  • FLJ38614SYNCI
DEFINITION
  • Human CHD2 wild-type allele is located in the vicinity of 15q26 and is approximately 125 kb in length. This allele, which encodes chromodomain-helicase-DNA-binding protein 2, may play a role in the modulation of both chromatin structure and gene expression. Deletion of this gene may be associated with congenital diaphragmatic hernia.NCIOMIM
code
  • C75308
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