COL1A1 Chromosome 17

Collagen type I alpha 1 chain
1224 variants 1224 Health Risk

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What This Gene Does
This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish, Feb 2008]
Gene Info
Gene Group
Fibrillar collagens
Locus Type
gene with protein product
Location
17q21.33
Ensembl
ENSG00000108821
Associated Conditions (67)
Bone mineral density variation quantitative trait locus
Osteogenesis imperfecta type I
Cardiovascular phenotype
Osteogenesis imperfecta
Infantile cortical hyperostosis
Ehlers-Danlos syndrome
arthrochalasia type
See cases
COL1A1-related disorder
Connective tissue disorder
2
Familial thoracic aortic aneurysm and aortic dissection
8 conditions
7 conditions
Hypertrophic cardiomyopathy
Keratoconus
Osteogenesis imperfecta with normal sclerae
dominant form
Colon adenocarcinoma
Familial cancer of breast
+47 more conditions
Key Variants
RS1107946
association
Bone mineral density variation quantitative trait locus, Bone mineral density variation quantitative trait locus
Health Risk
RS11327935
association
Bone mineral density variation quantitative trait locus, Bone mineral density variation quantitative trait locus
Health Risk
RS1800012
association
Bone mineral density variation quantitative trait locus, Bone mineral density variation quantitative trait locus
Health Risk
RS1009435359
Conflicting classifications of pathogenicity
Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
Health Risk
RS1014402681
Conflicting classifications of pathogenicity
Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
Health Risk
RS1033263382
Conflicting classifications of pathogenicity
Osteogenesis imperfecta type I, Cardiovascular phenotype, Osteogenesis imperfecta type I
Health Risk
RS1051473344
Conflicting classifications of pathogenicity
Osteogenesis imperfecta type I, Osteogenesis imperfecta, Infantile cortical hyperostosis
Health Risk
RS1061970
Conflicting classifications of pathogenicity
Infantile cortical hyperostosis, Ehlers-Danlos syndrome, arthrochalasia type
Health Risk
RS113950465
Conflicting classifications of pathogenicity
Osteogenesis imperfecta, Osteogenesis imperfecta type I, Cardiovascular phenotype
Health Risk
RS115997082
Conflicting classifications of pathogenicity
Ehlers-Danlos syndrome, arthrochalasia type, Infantile cortical hyperostosis
Health Risk
RS117672175
Conflicting classifications of pathogenicity
Osteogenesis imperfecta, Ehlers-Danlos syndrome, arthrochalasia type
Health Risk
RS1176922412
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Osteogenesis imperfecta type I, Cardiovascular phenotype
Health Risk
All Variants (1224)
RSID Category Clinical Significance Conditions
RS72651651 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS72651653 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS72651658 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta, 8 conditions
RS72651659 Health Risk Pathogenic
RS72651661 Health Risk Pathogenic Osteogenesis imperfecta with normal sclerae, dominant form, Osteogenesis imperfecta with normal sclerae
RS72651663 Health Risk Pathogenic
RS72651666 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72651667 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72653131 Health Risk Pathogenic Osteogenesis imperfecta with normal sclerae, dominant form, Osteogenesis imperfecta type III
RS72653133 Health Risk Pathogenic Osteogenesis imperfecta with normal sclerae, dominant form, Osteogenesis imperfecta type I
RS72653136 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta type I
RS72653137 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta type I
RS72653139 Health Risk Pathogenic Osteogenesis imperfecta, Osteogenesis imperfecta
RS72653140 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72653143 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS72653147 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta, Ehlers-Danlos syndrome
RS72653150 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta, Osteogenesis imperfecta type I
RS72653151 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72653152 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS72653154 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS72653155 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72653156 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72653166 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS72653168 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta, Osteogenesis imperfecta type I
RS72653170 Health Risk Pathogenic Infantile cortical hyperostosis, Osteogenesis imperfecta type I, 7 conditions
RS72653171 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72653172 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS72653173 Health Risk Pathogenic Osteogenesis imperfecta, Osteogenesis imperfecta type I, Ehlers-Danlos syndrome
RS72653175 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72653176 Health Risk Pathogenic
RS72653178 Health Risk Pathogenic Osteogenesis imperfecta type III, Osteogenesis imperfecta type I, Osteogenesis imperfecta
RS72654794 Health Risk Pathogenic Osteogenesis imperfecta type I, COL1A1-related disorder, Osteogenesis imperfecta type I
RS72654801 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72654802 Health Risk Pathogenic Osteogenesis imperfecta type I, COL1A1-related disorder, Osteogenesis imperfecta with normal sclerae
RS72656303 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS72656306 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS72656314 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta, Osteogenesis imperfecta type III
RS72656320 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72656321 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta
RS72656323 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72656324 Health Risk Pathogenic Osteogenesis imperfecta, perinatal lethal, Osteogenesis imperfecta type I
RS72656326 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta, Osteogenesis imperfecta type I
RS72656327 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72656331 Health Risk Pathogenic OSTEOGENESIS IMPERFECTA, TYPE IIC, OSTEOGENESIS IMPERFECTA
RS72656336 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72656337 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72656338 Health Risk Pathogenic Osteogenesis imperfecta with normal sclerae, dominant form, Osteogenesis imperfecta with normal sclerae
RS72656340 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
RS72656343 Health Risk Pathogenic Osteogenesis imperfecta type 2, thin-bone, Osteogenesis imperfecta type I
RS72656348 Health Risk Pathogenic Osteogenesis imperfecta type I, Osteogenesis imperfecta type I
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