COL9A1 Chromosome 6

Collagen type IX alpha 1 chain
116 variants 116 Health Risk

Upload your DNA to see your personal genotypes for variants in COL9A1.

What This Gene Does
This gene encodes one of the three alpha chains of type IX collagen, which is a minor (5-20%) collagen component of hyaline cartilage. Type IX collagen is usually found in tissues containing type II collagen, a fibrillar collagen. Studies in knockout mice have shown that synthesis of the alpha 1 chain is essential for assembly of type IX collagen molecules, a heterotrimeric molecule, and that lack of type IX collagen is associated with early onset osteoarthritis. Mutations in this gene are associated with osteoarthritis in humans, with multiple epiphyseal dysplasia, 6, a form of chondrodysplasia, and with Stickler syndrome, a disease characterized by ophthalmic, orofacial, articular, and auditory defects. Two transcript variants that encode different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Collagen proteoglycans|Fibril associated collagens with interrupted triple helices"
Locus Type
gene with protein product
Location
6q13
Ensembl
ENSG00000112280
Associated Conditions (17)
Connective tissue disorder
Inborn genetic diseases
COL9A1-related disorder
Epiphyseal dysplasia
multiple
6
Stickler syndrome
type 4
Hearing impairment
Optic atrophy
Retinal dystrophy
Uterine corpus endometrial carcinoma
Familial cancer of breast
Congenital heart disease
Marfan syndrome
See cases
Sensorineural hearing loss disorder
Key Variants
All Variants (116)
RSID Category Clinical Significance Conditions
RS1135057 Health Risk Conflicting classifications of pathogenicity Connective tissue disorder, Connective tissue disorder
RS1360782538 Health Risk Conflicting classifications of pathogenicity
RS138583508 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, COL9A1-related disorder, Epiphyseal dysplasia
RS140274454 Health Risk Conflicting classifications of pathogenicity
RS141047907 Health Risk Conflicting classifications of pathogenicity
RS141776183 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS141825151 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS141830060 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS142328549 Health Risk Conflicting classifications of pathogenicity
RS143848379 Health Risk Conflicting classifications of pathogenicity Epiphyseal dysplasia, multiple, 6
RS144581626 Health Risk Conflicting classifications of pathogenicity Hearing impairment, Hearing impairment
RS145698301 Health Risk Conflicting classifications of pathogenicity Stickler syndrome, type 4, Epiphyseal dysplasia
RS146700420 Health Risk Conflicting classifications of pathogenicity COL9A1-related disorder, COL9A1-related disorder
RS147237457 Health Risk Conflicting classifications of pathogenicity Stickler syndrome, type 4, Stickler syndrome
RS147747530 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS149389568 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS149459564 Health Risk Conflicting classifications of pathogenicity COL9A1-related disorder, Inborn genetic diseases, COL9A1-related disorder
RS149830493 Health Risk Conflicting classifications of pathogenicity Epiphyseal dysplasia, multiple, 6
RS150026024 Health Risk Conflicting classifications of pathogenicity
RS150571620 Health Risk Conflicting classifications of pathogenicity
RS151129325 Health Risk Conflicting classifications of pathogenicity COL9A1-related disorder, COL9A1-related disorder
RS192047082 Health Risk Conflicting classifications of pathogenicity Hearing impairment, Stickler syndrome, type 4
RS192467838 Health Risk Conflicting classifications of pathogenicity Optic atrophy, Retinal dystrophy, Optic atrophy
RS200018557 Health Risk Conflicting classifications of pathogenicity
RS200829297 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Stickler syndrome, Retinal dystrophy
RS201480339 Health Risk Conflicting classifications of pathogenicity Connective tissue disorder, Connective tissue disorder
RS202176764 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, COL9A1-related disorder, Stickler syndrome
RS202232444 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS367798424 Health Risk Conflicting classifications of pathogenicity COL9A1-related disorder, COL9A1-related disorder
RS369698214 Health Risk Conflicting classifications of pathogenicity Familial cancer of breast, Familial cancer of breast
RS372320539 Health Risk Conflicting classifications of pathogenicity Congenital heart disease, Inborn genetic diseases, Congenital heart disease
RS376664058 Health Risk Conflicting classifications of pathogenicity
RS527945609 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS535866098 Health Risk Conflicting classifications of pathogenicity
RS540419799 Health Risk Conflicting classifications of pathogenicity COL9A1-related disorder, COL9A1-related disorder
RS552818441 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS557157592 Health Risk Conflicting classifications of pathogenicity
RS564421091 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS755501266 Health Risk Conflicting classifications of pathogenicity
RS760704462 Health Risk Conflicting classifications of pathogenicity
RS762825632 Health Risk Conflicting classifications of pathogenicity
RS768737537 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS773143381 Health Risk Conflicting classifications of pathogenicity COL9A1-related disorder, COL9A1-related disorder
RS773380068 Health Risk Conflicting classifications of pathogenicity Marfan syndrome, Marfan syndrome
RS774856588 Health Risk Conflicting classifications of pathogenicity
RS1064797325 Health Risk Likely pathogenic
RS1322800124 Health Risk Likely pathogenic
RS1322829123 Health Risk Likely pathogenic
RS1490405035 Health Risk Likely pathogenic
RS1562305261 Health Risk Likely pathogenic
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