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
Exon/intron information NM_020638.2 exon/intron table
Associated with diseases ADHR, HFTC, HFTC2, HR
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 18
Unique public DNA variants reported 8
Individuals with public variants 13
Hidden variants 1
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated January 31, 2022
Version FGF23:220131

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_020638.2.
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
Homepage URL https://www.LOVD.nl/FGF23
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))
HFTC2 (Tumoral calcinosis, hyperphosphatemic, familial, 2)
HGMD FGF23
GeneCards FGF23
GeneTests FGF23
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 18


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