About: CYP26B1 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
  • CYP26B1 wt Allele
rdfs:subClassOf
OMIM_Number
  • 605207
GenBank_Accession_Number
  • NM_019885
Semantic_Type
  • Gene or Genome
Preferred_Name
  • CYP26B1 wt Allele
EntrezGene_ID
  • 56603
HGNC_ID
  • HGNC:20581
FULL_SYN
  • Cytochrome P450, Family 26, Subfamily B, Polypeptide 1 wt AlleleSYNCI
  • RHFCASYNCI
  • CYP26B1 wt AllelePTNCI
  • CYP26A2SYNCI
  • P450RAI2SYNCI
  • P450RAI-2SYNCI
DEFINITION
  • Human CYP26B1 wild-type allele is located in the vicinity of 2p13.2 and is approximately 19 kb in length. This allele, which encodes cytochrome P450 26B1 protein, is involved in the specific inactivation of all-trans-retinoic acid. Mutations in this gene are associated with craniofacial and other skeletal anomalies.NCI
code
  • C104875
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