About: STIL 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
  • STIL wt Allele
equivalentClass
OMIM_Number
  • 181590
GenBank_Accession_Number
  • M74558
Semantic_Type
  • Gene or Genome
Preferred_Name
  • STIL wt Allele
NCI_META_CUI
  • CL435371
EntrezGene_ID
  • 6491
HGNC_ID
  • HGNC:10879
FULL_SYN
  • SILSYNCI
  • STIL wt AllelePTNCI
  • SCL/TAL1 Interrupting Locus wt AlleleSYNCI
  • MCPH7SYNCI
  • RP1-18D14.8SYNCI
DEFINITION
  • Human STIL wild-type allele is located in the vicinity of 1p32 and is approximately 64 kb in length. This allele, which encodes SCL-interrupting locus protein, is involved in signaling that promotes cellular proliferation and modulates embryonic development. A chromosomal deletion at 1p32 between this gene and the TAL1 gene is associated with T-cell acute lymphoblastic leukemia. Mutation of the gene is associated with microcephaly primary type 7.NCI
code
  • C101127
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