rs144170209

This variant is located in the COMP gene.

ClinVar annotation

Uncertain Significance★★★
3 submitters1 publication

Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome; Multiple epiphyseal dysplasia type 1; not provided

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About COMP

The protein encoded by this gene is a noncollagenous extracellular matrix (ECM) protein. It consists of five identical glycoprotein subunits, each with EGF-like and calcium-binding (thrombospondin-like) domains. Oligomerization results from formation of a five-stranded coiled coil and disulfides. Binding to other ECM proteins such as collagen appears to depend on divalent cations. Contraction or expansion of a 5 aa aspartate repeat and other mutations can cause pseudochondroplasia (PSACH) and multiple epiphyseal dysplasia (MED). [provided by RefSeq, Jul 2016]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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