The MESP2 gene homepage

General information
Gene symbol MESP2
Gene name mesoderm posterior 2 homolog (mouse)
Chromosome 15
Chromosomal band q26.1
Imprinted Unknown
Genomic reference NG_008608.1
Transcript reference NM_001039958.1
Associated with diseases SCDO1, SCDO2
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 17
Unique public DNA variants reported 16
Individuals with public variants 2
Hidden variants 2
Date created May 03, 2013
Date last updated April 19, 2024
Version MESP2:240419

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 29659
Entrez Gene 145873
PubMed articles MESP2
OMIM - Gene 605195
OMIM - Diseases SCDO1 (dysostosis, spondylocostal, autosomal recessive, type 1 (SCDO-1, Jarcho-Levin syndrome))
SCDO2 (dysostosis, spondylocostal, autosomal recessive, type 2 (SCDO-2))
Orphanet MESP2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00012014 15 mesoderm posterior 2 homolog (mouse) NM_001039958.1 NP_001035047.1 17


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