The FRA10AC1 gene homepage

General information
Gene symbol FRA10AC1
Gene name fragile site, folic acid type, rare, fra(10)(q23.3) or fra(10)(q24.2) candidate 1
Chromosome 10
Chromosomal band q23.33
Imprinted Unknown
Genomic reference NC_000010.10
Transcript reference NM_145246.4
Exon/intron information NM_145246.4 exon/intron table
Associated with diseases NDD, NEDGFC
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 24
Unique public DNA variants reported 17
Individuals with public variants 12
Hidden variants -
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 May 05, 2025
Version FRA10AC1:250505

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_145246.4.
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 http://www.LOVD.nl/FRA10AC1
HGNC HGNC:1162
Entrez Gene 118924
PubMed articles FRA10AC1
OMIM - Gene 608866
OMIM - Diseases NEDGFC (neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities)
HGMD FRA10AC1
GeneCards FRA10AC1
NIH Genetic Testing Registry FRA10AC1
Orphanet FRA10AC1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00008127 10 fragile site, folic acid type, rare, fra(10)(q23.3) or fra(10)(q24.2) candidate 1 NM_145246.4 NP_660289.2 24


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