COL27A1 Chromosome 9

Collagen type XXVII alpha 1 chain
179 variants 179 Health Risk

Upload your DNA to see your personal genotypes for variants in COL27A1.

What This Gene Does
This gene encodes a member of the fibrillar collagen family, and plays a role during the calcification of cartilage and the transition of cartilage to bone. The encoded protein product is a preproprotein. It includes an N-terminal signal peptide, which is followed by an N-terminal propetide, mature peptide and a C-terminal propeptide. The N-terminal propeptide contains thrombospondin N-terminal-like and laminin G-like domains. The mature peptide is a major triple-helical region. The C-terminal propeptide, also known as COLFI domain, plays crucial roles in tissue growth and repair. Mutations in this gene cause Steel syndrome. Alternatively spliced transcript variants have been found, but the full-length nature of some variants has not been determined. [provided by RefSeq, Sep 2014]
Gene Info
Gene Group
"MicroRNA protein coding host genes|Fibrillar collagens"
Locus Type
gene with protein product
Location
9q32
Ensembl
ENSG00000196739
Associated Conditions (8)
Inborn genetic diseases
COL27A1-related disorder
Steel syndrome
Clear cell carcinoma of kidney
Familial cancer of breast
Thyroid cancer
nonmedullary
1
Key Variants
All Variants (179)
RSID Category Clinical Significance Conditions
RS2490407204 Health Risk Pathogenic
RS2490418448 Health Risk Pathogenic
RS2490483848 Health Risk Pathogenic
RS2490484546 Health Risk Pathogenic
RS2490546871 Health Risk Pathogenic
RS2490556729 Health Risk Pathogenic
RS2490558508 Health Risk Pathogenic
RS2490561736 Health Risk Pathogenic
RS2490569167 Health Risk Pathogenic
RS2490582353 Health Risk Pathogenic
RS2491028292 Health Risk Pathogenic
RS2491109427 Health Risk Pathogenic
RS2491340979 Health Risk Pathogenic
RS2491397213 Health Risk Pathogenic
RS2491405260 Health Risk Pathogenic
RS2491545342 Health Risk Pathogenic
RS2491546539 Health Risk Pathogenic
RS5900078 Health Risk Pathogenic Steel syndrome, Steel syndrome
RS753461513 Health Risk Pathogenic Steel syndrome, Steel syndrome
RS764305873 Health Risk Pathogenic
RS773501392 Health Risk Pathogenic Steel syndrome, Steel syndrome
RS778661695 Health Risk Pathogenic
RS940642841 Health Risk Pathogenic
RS1328051341 Health Risk Pathogenic/Likely pathogenic Steel syndrome, Steel syndrome
RS1465820080 Health Risk Pathogenic/Likely pathogenic Steel syndrome, Steel syndrome
RS1564576546 Health Risk Pathogenic/Likely pathogenic Steel syndrome, Steel syndrome
RS1835450838 Health Risk Pathogenic/Likely pathogenic Steel syndrome, Steel syndrome
RS1849088219 Health Risk Pathogenic/Likely pathogenic Steel syndrome, Steel syndrome
RS2135531602 Health Risk Pathogenic/Likely pathogenic Steel syndrome, Steel syndrome
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