About: SH3D19 wt Allele     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz:8890 associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • SH3D19 wt Allele
rdfs:subClassOf
OMIM_Number
  • 608674
GenBank_Accession_Number
  • BX647422
Semantic_Type
  • Gene or Genome
Preferred_Name
  • SH3D19 wt Allele
NCI_META_CUI
  • CL430714
EntrezGene_ID
  • 152503
HGNC_ID
  • HGNC:30418
FULL_SYN
  • SH3 Domain Containing 19 wt AlleleSYNCI
  • DKFZp434D0215SYNCI
  • EEN Binding Protein GeneSYNCI
  • EBPSYNCI
  • SH3D19 wt AllelePTNCI
  • EVE1SYNCI
  • KrynSYNCI
  • SH3P19SYNCI
  • MGC105136SYNCI
  • MGC118910SYNCI
  • MGC118911SYNCI
  • MGC118912SYNCI
  • MGC118913SYNCI
DEFINITION
  • Human SH3D19 wild-type allele is located in the vicinity of 4q31.3 and is approximately 108 kb in length. This allele, which encodes SH3 domain-containing protein 19, plays a role in both protein-protein interactions and protein localization to the plasma membrane. A translocation involving this gene and the RUNX1 gene may be associated with acute myeloid leukemia.NCI
code
  • C98006
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