About: STIL wt Allele     Goto   Sponge   Distinct   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
Faceted Search & Find service v1.16.118 as of Jun 21 2024


Alternative Linked Data Documents: ODE     Content Formats:   [cxml] [csv]     RDF   [text] [turtle] [ld+json] [rdf+json] [rdf+xml]     ODATA   [atom+xml] [odata+json]     Microdata   [microdata+json] [html]    About   
This material is Open Knowledge   W3C Semantic Web Technology [RDF Data] Valid XHTML + RDFa
OpenLink Virtuoso version 07.20.3240 as of Jun 21 2024, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (126 GB total memory, 83 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software