About: ZMYM3 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
  • ZMYM3 wt Allele
rdfs:subClassOf
OMIM_Number
  • 300061
GenBank_Accession_Number
  • AB002383
Semantic_Type
  • Gene or Genome
Preferred_Name
  • ZMYM3 wt Allele
NCI_META_CUI
  • CL435940
EntrezGene_ID
  • 9203
HGNC_ID
  • HGNC:13054
FULL_SYN
  • Zinc Finger, MYM-Type 3 wt AlleleSYNCI
  • MYMSYNCI
  • ZMYM3 wt AllelePTNCI
  • XFIMSYNCI
  • ZNF261SYNCI
  • KIAA0385SYNCI
  • DXS6673ESYNCI
  • ZNF198L2SYNCI
DEFINITION
  • Human ZMYM3 wild-type allele is located in the vicinity of Xq13.1 and is approximately 16 kb in length. This allele, which encodes zinc finger MYM-type protein 3, plays a role in the regulation of chromatin remodeling, cell morphology and cytoskeletal organization. A chromosomal translocation (X;13) involving this gene is associated with X-linked mental retardation.NCI
DesignNote
  • Mutation of the ZMYM3 gene may be associated with chronic lymphocytic leukemia. (N Engl J Med 2011; 365:2497-2506.)
code
  • C101618
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