The MSX1 gene homepage

General information
Gene symbol MSX1
Gene name msh homeobox 1
Chromosome 4
Chromosomal band p16.2
Imprinted Unknown
Genomic reference NG_008121.1
Transcript reference NM_002448.3
Associated with diseases HNPCC
Citation reference(s) -
Curators (1) MyHVP
Total number of public variants reported 10
Unique public DNA variants reported 6
Individuals with public variants 7
Hidden variants 2
Date created November 19, 2017
Date last updated September 08, 2021
Version MSX1:210908

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 7391
Entrez Gene 4487
PubMed articles MSX1
OMIM - Gene 142983
OMIM - Diseases HNPCC (Lynch syndrome)


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000003 4 msh homeobox 1 NM_002448.3 NP_002439.2 10


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