ADAMTS18 Chromosome 16

ADAM metallopeptidase with thrombospondin type 1 motif 18
64 variants 64 Health Risk

Upload your DNA to see your personal genotypes for variants in ADAMTS18.

What This Gene Does
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature protein, which may regulate hemostatic balance and function as a tumor suppressor. Mutations in this gene may be associated with microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) and cone-rod dystrophy in human patients. [provided by RefSeq, May 2016]
Gene Info
Gene Group
ADAM metallopeptidases with thrombospondin type 1 motif
Locus Type
gene with protein product
Location
16q23.1
Ensembl
ENSG00000140873
Associated Conditions (7)
Retinitis pigmentosa
Inborn genetic diseases
Microcornea-myopic chorioretinal atrophy
Retinal dystrophy
ADAMTS18-related disorder
Familial cancer of breast
Retinal disorder
Key Variants
RS138435590
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Inborn genetic diseases, Microcornea-myopic chorioretinal atrophy
Health Risk
RS139553755
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS141026455
Conflicting classifications of pathogenicity
ADAMTS18-related disorder, Inborn genetic diseases, ADAMTS18-related disorder
Health Risk
RS141796905
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS143359890
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS143757943
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1451891780
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS145823665
Conflicting classifications of pathogenicity
ADAMTS18-related disorder, Inborn genetic diseases, ADAMTS18-related disorder
Health Risk
RS148703569
Conflicting classifications of pathogenicity
Microcornea-myopic chorioretinal atrophy, Retinitis pigmentosa, ADAMTS18-related disorder
Health Risk
RS183006469
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS201193356
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS202020248
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
All Variants (64)
RSID Category Clinical Significance Conditions
RS397515469 Health Risk Pathogenic Microcornea-myopic chorioretinal atrophy, Microcornea-myopic chorioretinal atrophy
RS747773771 Health Risk Pathogenic
RS751029682 Health Risk Pathogenic
RS760304370 Health Risk Pathogenic
RS762638651 Health Risk Pathogenic
RS763330900 Health Risk Pathogenic
RS764863191 Health Risk Pathogenic
RS775431905 Health Risk Pathogenic
RS776870884 Health Risk Pathogenic Microcornea-myopic chorioretinal atrophy, Microcornea-myopic chorioretinal atrophy
RS777518062 Health Risk Pathogenic
RS868732406 Health Risk Pathogenic
RS1195694707 Health Risk Pathogenic/Likely pathogenic
RS139516327 Health Risk Pathogenic/Likely pathogenic Microcornea-myopic chorioretinal atrophy, Retinal disorder, Microcornea-myopic chorioretinal atrophy
RS935159456 Health Risk Pathogenic/Likely pathogenic ADAMTS18-related disorder, ADAMTS18-related disorder
Sign Up to Analyze Your DNA Log In