View MSX2 gene homepage

General information
Gene symbol MSX2
Gene name msh homeobox 2
Chromosome 5
Chromosomal band q35.2
Imprinted Unknown
Genomic reference NG_008124.1
Transcript reference NM_002449.4
Associated with diseases CRS-2, Parietal foramina, Parietal foramina with cleidocranial dysplasia
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 1
Unique public DNA variants reported 1
Individuals with public variants 1
Hidden variants 0
Date created May 03, 2013

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
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
HGNC 7392
Entrez Gene 4488
PubMed articles MSX2
OMIM - Gene 123101
OMIM - Diseases CRS-2 (craniosynostosis, type 2 (CRS-2))
Parietal foramina
Parietal foramina with cleidocranial dysplasia

Active transcripts




NCBI ID     

NCBI Protein ID     

00013979 5 msh homeobox 2 NM_002449.4 NP_002440.2 1