Gene entry

MESP2

mesoderm posterior bHLH transcription factor 2

Chromosome: 15
Cytoband: 15q26.1
Variants (rsID): 3

MESP2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q26.1). Its official name is “mesoderm posterior bHLH transcription factor 2”. The reference table lists 3 variants (rsID) for this gene.

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Clinically classified variants

2 reference-table entries with clinical significance.

rs185706635Benignsingle nucleotide variantSpondylocostal dysostosis 2, autosomal recessive
rs28462216Benignsingle nucleotide variantSpondylocostal dysostosis 2, autosomal recessive

Other listed variants

rs12908343

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.