COL4A5 Chromosome X

Collagen type IV alpha 5 chain
1069 variants 1069 Health Risk

Upload your DNA to see your personal genotypes for variants in COL4A5.

What This Gene Does
This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. Mutations in this gene are associated with X-linked Alport syndrome, also known as hereditary nephritis. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Aug 2010]
Gene Info
Gene Group
Network forming collagens
Locus Type
gene with protein product
Location
Xq22.3
Ensembl
ENSG00000188153
Associated Conditions (36)
X-linked Alport syndrome
Alport syndrome
COL4A5-related disorder
Inborn genetic diseases
Autosomal dominant Alport syndrome
Lung cancer
See cases
Kidney disorder
Thyroid cancer
nonmedullary
1
Hearing impairment
Disease of glomerular basement membrane
Rare disease with thoracic aortic aneurysm and aortic dissection
Microscopic hematuria
Hematuria
Familial hematuria
Steroid-resistant nephrotic syndrome
Proteinuria
Rare genetic deafness
+16 more conditions
Key Variants
All Variants (1069)
RSID Category Clinical Significance Conditions
RS2068717187 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2068717619 Health Risk Pathogenic Alport syndrome, Alport syndrome
RS2147448022 Health Risk Pathogenic
RS2147448071 Health Risk Pathogenic
RS2147657763 Health Risk Pathogenic
RS2147722166 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147746317 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147746687 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147754967 Health Risk Pathogenic X-linked Alport syndrome, Nonpapillary renal cell carcinoma, X-linked Alport syndrome
RS2147759174 Health Risk Pathogenic
RS2147770199 Health Risk Pathogenic
RS2147776527 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147776565 Health Risk Pathogenic
RS2147776596 Health Risk Pathogenic
RS2147776797 Health Risk Pathogenic Hepatocellular carcinoma, Hepatocellular carcinoma
RS2147777495 Health Risk Pathogenic Alport syndrome, Alport syndrome
RS2147784271 Health Risk Pathogenic
RS2147787972 Health Risk Pathogenic
RS2147788229 Health Risk Pathogenic
RS2147788399 Health Risk Pathogenic
RS2147796671 Health Risk Pathogenic
RS2147798059 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147798143 Health Risk Pathogenic
RS2147798207 Health Risk Pathogenic
RS2147798228 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147809070 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147809078 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147809122 Health Risk Pathogenic
RS2147810144 Health Risk Pathogenic
RS2147813799 Health Risk Pathogenic
RS2147819501 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147820825 Health Risk Pathogenic
RS2147820991 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147831991 Health Risk Pathogenic
RS2147832420 Health Risk Pathogenic
RS2147849950 Health Risk Pathogenic
RS2147850123 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147859836 Health Risk Pathogenic
RS2147860367 Health Risk Pathogenic
RS2147865567 Health Risk Pathogenic
RS2147865716 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147865795 Health Risk Pathogenic
RS2147865884 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147869121 Health Risk Pathogenic
RS2147869202 Health Risk Pathogenic
RS2147869275 Health Risk Pathogenic X-linked Alport syndrome, X-linked Alport syndrome
RS2147872098 Health Risk Pathogenic
RS2147872148 Health Risk Pathogenic
RS2147872245 Health Risk Pathogenic
RS2147872357 Health Risk Pathogenic
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