About: UGT2B17 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
  • UGT2B17 wt Allele
rdfs:subClassOf
OMIM_Number
  • 601903
GenBank_Accession_Number
  • U59209
Semantic_Type
  • Gene or Genome
Preferred_Name
  • UGT2B17 wt Allele
EntrezGene_ID
  • 7367
HGNC_ID
  • HGNC:12547
FULL_SYN
  • UDP Glucuronosyltransferase 2 Family, Polypeptide B17 wt AlleleSYNCI
  • UGT2B17 wt AllelePTNCI
  • UDPGT2B17SYNCI
DEFINITION
  • Human UGT2B17 wild-type allele is located in the vicinity of 4q13 and is approximately 31 kb in length. This allele, which encodes UDP-glucuronosyltransferase 2B17 protein, is involved in the catabolism of xenobiotics and steroids. Copy number variation of the gene is associated with aberrant bone mineral density quantitative trait which can lead to osteoporosis.NCI
code
  • C105424
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, 48 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software