The RAC3 gene homepage

General information
Gene symbol RAC3
Gene name ras-related C3 botulinum toxin substrate 3 (rho family, small GTP binding protein Rac3)
Chromosome 17
Chromosomal band q25.3
Imprinted Unknown
Genomic reference NC_000017.10
Transcript reference NM_005052.2
Exon/intron information NM_005052.2 exon/intron table
Associated with diseases NEDBAF
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 18
Hidden variants 4
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 RAC3:250505

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_005052.2.
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/RAC3
HGNC HGNC:9803
Entrez Gene 5881
PubMed articles RAC3
OMIM - Gene 602050
OMIM - Diseases NEDBAF (Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies)
HGMD RAC3
GeneCards RAC3
NIH Genetic Testing Registry RAC3
Orphanet RAC3


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00017352 17 ras-related C3 botulinum toxin substrate 3 (rho family, small GTP binding protein Rac3) NM_005052.2 NP_005043.1 24


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