rs886049441
This variant is located in the COL2A1 gene.
▶ClinVar annotation
Stickler syndrome type 1; Type 2 collagenopathy
View on ClinVar →About COL2A1
This gene encodes the alpha-1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye. Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type. In addition, defects in processing chondrocalcin, a calcium binding protein that is the C-propeptide of this collagen molecule, are also associated with chondrodysplasia. There are two transcripts identified for this gene. [provided by RefSeq, Jul 2008]
View all COL2A1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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