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, PFM, PFMCCD
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants 0
Date created May 03, 2013

Links to other resources
HGNC 7392
Entrez Gene 4488
PubMed articles MSX2
OMIM - Gene 123101
OMIM - Diseases CRS-2 (craniosynostosis, type 2 (CRS-2))
PFM (foramina, parietal (PFM))
PFMCCD (foramina, parietal, with cleidocranial dysplasia (PFMCCD))

Active transcripts




NCBI ID     

NCBI Protein ID     

00013979 5 msh homeobox 2 NM_002449.4 NP_002440.2 0