Entity Details
Details
PrimaryID | 145873 |
RefseqGene | NG_008608 |
Symbol | MESP2 |
Name | mesoderm posterior bHLH transcription factor 2 |
Chromosome | 15 |
Location | 15q26.1 |
TaxID | 9606 |
Status | live |
SourceGenome | genomic |
SourceOrigin | natural |
CreationDate | 2002-01-21 |
ModificationDate | 2021-06-11 |
Diseases
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Disease ID | Source | Name | Description |
608681 | OMIM | Spondylocostal dysostosis 2, autosomal recessive (SCDO2) | A condition of variable severity associated with vertebral and rib segmentation defects. The main skeletal malformations include fusion of vertebrae, hemivertebrae, fusion of certain ribs, and other rib malformations. Deformity of the chest and spine (severe scoliosis, kyphoscoliosis and lordosis) is a natural consequence of the malformation and leads to a dwarf-like appearance. As the thorax is small, infants frequently have respiratory insufficiency and repeated respiratory infections resulting in life-threatening complications in the first year of life. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
3 interactions