About: KLLN 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
  • KLLN wt Allele
rdfs:subClassOf
OMIM_Number
  • 612105
GenBank_Accession_Number
  • EU552092
Semantic_Type
  • Gene or Genome
Preferred_Name
  • KLLN wt Allele
NCI_META_CUI
  • CL426728
EntrezGene_ID
  • 100144748
HGNC_ID
  • HGNC:37212
FULL_SYN
  • KLLN wt AllelePTNCI
  • KLNSYNCI
  • Killin, p53-Regulated DNA Replication Inhibitor wt AlleleSYNCI
  • KILLINSYNCI
  • Killin Protein GeneSYNCI
DEFINITION
  • Human KILLIN wild-type allele is located in the vicinity of 10q23 and is approximately 4 kb in length. This allele, which encodes killin protein, plays a role in both DNA binding and the mediation of p53-mediated apoptosis.NCI
DesignNote
  • Methylation of the KILLIN gene promoter may be associated with Cowden syndrome, Cowden-like syndrome and cancer susceptibility. (JAMA. 2010; 304:2724-2731.)
  • The human KILLIN gene shares promoter sequences with the human PTEN gene. (OMIM)
code
  • C95287
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