About: NOTCH2 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
  • NOTCH2 wt Allele
rdfs:subClassOf
OMIM_Number
  • 600275
GenBank_Accession_Number
  • AF315356
Semantic_Type
  • Gene or Genome
Preferred_Name
  • NOTCH2 wt Allele
NCI_META_CUI
  • CL430468
EntrezGene_ID
  • 4853
HGNC_ID
  • HGNC:7882
FULL_SYN
  • Notch Homolog 2 (Drosophila) GeneSYNCI
  • hN2SYNCI
  • AGS2SYNCI
  • NOTCH2 wt AllelePTNCI
  • HJCYSSYNCI
  • Notch 2 wt AlleleSYNCI
DEFINITION
  • Human NOTCH2 wild-type allele is located within 1p13-p11 and is approximately 158 kb in length. This allele, which encodes neurogenic locus notch homolog protein 2, is involved in the mediation of cell-cell signaling. Mutation of the gene is associated with both Alagille syndrome type 2 and Hajdu-Cheney syndrome.NCI
code
  • C97678
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, 117 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software