Terminology Service for NFDI4Health

LCN2 wt Allele

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Human LCN2 wild-type allele is located in the vicinity of 9q34 and is approximately 5 kb in length. This allele, which encodes neutrophil gelatinase-associated lipocalin protein, may be involved in both the modulation of inflammation and the regulation of the transport of hydrophobic substances (ie. retinol, lipopolysaccharide). The expression of this gene may be elevated in many cancers and inflammatory diseases. [ ]

Term info

Label

LCN2 wt Allele

Synonyms
  • 24p3
  • HNL
  • LCN2 wt Allele
  • Lipocalin 2 (Oncogene 24p3) Gene
  • Lipocalin 2 wt Allele
  • MSFI
  • NGAL
Subsets

NCIT_C116977, NCIT_C142800, NCIT_C142799

Display Name

LCN2 wt Allele

Legacy Concept Name

LCN2_wt_Allele

OMIM Number

600181

Preferred Name

LCN2 wt Allele

Semantic Type

Gene or Genome

UMLS CUI

C2346625

code

C71436

Term relations