About: FGF23 wt Allele     Goto   Sponge   Distinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • FGF23 wt Allele
rdfs:subClassOf
OMIM_Number
  • 605380
GenBank_Accession_Number
  • AF263537
Semantic_Type
  • Gene or Genome
Preferred_Name
  • FGF23 wt Allele
EntrezGene_ID
  • 8074
HGNC_ID
  • HGNC:3680
FULL_SYN
  • ADHRSYNCI
  • FGF23 wt AllelePTNCI
  • Fibroblast Growth Factor 23 wt AlleleSYNCI
  • HYPFSYNCI
  • HPDR2SYNCI
  • PHPTCSYNCI
  • FGF-23SYNCI
DEFINITION
  • Human FGF23 wild-type allele is located in the vicinity of 12p13.3 and is approximately 12 kb in length. This allele, which encodes fibroblast growth factor 23 protein, plays a role in regulation of phosphate homeostasis. Mutations in this gene are associated with autosomal dominant hypophosphatemic rickets (ADHR) and familial tumoral calcinosis with hyperphosphatemia. It is overexpressed in oncogenic hypophosphatemic osteomalacia (OHO).NCI
code
  • C104383
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