About: LCLAT1 wt Allele     Goto   Sponge   Distinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • LCLAT1 wt Allele
rdfs:subClassOf
OMIM_Number
  • 614241
GenBank_Accession_Number
  • AK095284
Semantic_Type
  • Gene or Genome
Preferred_Name
  • LCLAT1 wt Allele
NCI_META_CUI
  • CL437385
EntrezGene_ID
  • 253558
HGNC_ID
  • HGNC:26756
FULL_SYN
  • Lysocardiolipin Acyltransferase 1 wt AlleleSYNCI
  • UNQ1849/PRO3579SYNCI
  • LCLAT1 wt AllelePTNCI
  • LYCATSYNCI
  • ALCAT1SYNCI
  • AGPAT8SYNCI
  • UNQ1849SYNCI
  • 1AGPAT8SYNCI
  • HSRG1849SYNCI
DEFINITION
  • Human LCLAT1 wild-type allele is located in the vicinity of 2p23.1 and is approximately 197 kb in length. This allele, which encodes lysocardiolipin acyltransferase 1 protein, is involved in the modification of phospholipids.NCI
DesignNote
  • An intrachromosomal translocation resulting in a fusion between the LCLAT1 and ERBB4 genes may be associated with medulloblastoma. (Nature. 2012; 488:100-105.)
code
  • C102934
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