The FGF23 gene homepage

General information
Gene symbol FGF23
Gene name fibroblast growth factor 23
Chromosome 12
Chromosomal band p13
Imprinted Unknown
Genomic reference NG_007087.1
Transcript reference NM_020638.2
Associated with diseases ADHR, HFTC
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 6
Unique public DNA variants reported 5
Individuals with public variants 0
Hidden variants 1
Date created May 03, 2013
Date last updated September 15, 2020
Version FGF23:200915

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 3680
Entrez Gene 8074
PubMed articles FGF23
OMIM - Gene 605380
OMIM - Diseases ADHR (rickets, hypophosphatemic, autosomal dominant (ADHR))
HFTC (calcinosis, tumoral, hyperphosphatemic, familial (HFTC))
Orphanet FGF23


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00007929 12 fibroblast growth factor 23 NM_020638.2 NP_065689.1 6


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