The SATB2 gene homepage

General information
Gene symbol SATB2
Gene name SATB homeobox 2
Chromosome 2
Chromosomal band q33.1
Imprinted Unknown
Genomic reference NG_016976.1
Transcript reference NM_001172509.1
Exon/intron information NM_001172509.1 exon/intron table
Associated with diseases CPI, GLASS, ID
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) YA Zarate
Total number of public variants reported 178
Unique public DNA variants reported 106
Individuals with public variants 152
Hidden variants 7
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created May 01, 2012
Date last updated September 15, 2020
Version SATB2:200915

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_001172509.1.
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
HGNC 21637
Entrez Gene 23314
PubMed articles SATB2
OMIM - Gene 608148
OMIM - Diseases CPI (CPO)
GLASS (syndrome, Glass (GLASS, chromosome 2q32-q33 deletion syndrome))
GeneCards SATB2
GeneTests SATB2

Active transcripts




NCBI ID     

NCBI Protein ID     

00000163 2 SATB homeobox 2 NM_001172509.1 NP_056080.1 178

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