The SBF1 gene homepage

General information
Gene symbol SBF1
Gene name SET binding factor 1
Chromosome 22
Chromosomal band q13.33
Imprinted Unknown
Genomic reference NG_041810.1
Transcript reference NM_002972.2
Exon/intron information NM_002972.2 exon/intron table
Associated with diseases CMT4B3
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 196
Unique public DNA variants reported 167
Individuals with public variants 11
Hidden variants 13
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated April 19, 2024
Version SBF1:240419

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_002972.2.
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/SBF1
HGNC 10542
Entrez Gene 6305
PubMed articles SBF1
OMIM - Gene 603560
OMIM - Diseases CMT4B3 (Charcot-Marie-Tooth disease, type 4B3 (CMT-4B3))
HGMD SBF1
GeneCards SBF1
GeneTests SBF1
Orphanet SBF1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00018430 22 SET binding factor 1 NM_002972.2 NP_002963.2 196


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