COL4A4 Chromosome 2

Collagen type IV alpha 4 chain
776 variants 776 Health Risk

Upload your DNA to see your personal genotypes for variants in COL4A4.

What This Gene Does
This gene encodes one of the six subunits of type IV collagen, the major structural component of basement membranes. This particular collagen IV subunit, however, is only found in a subset of basement membranes. 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. Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease). Two transcripts, differing only in their transcription start sites, have been identified for this gene and, as is common for collagen genes, multiple polyadenylation sites are found in the 3' UTR. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Network forming collagens
Locus Type
gene with protein product
Location
2q36.3
Ensembl
ENSG00000081052
Associated Conditions (36)
Autosomal recessive Alport syndrome
Hematuria
benign familial
1
COL4A4-related disorder
Alport syndrome
Kidney disorder
Inborn genetic diseases
Meniere disease
Autosomal dominant Alport syndrome
Atypical hemolytic-uremic syndrome
Microscopic hematuria
Benign familial hematuria
Gastric cancer
Ovarian serous cystadenocarcinoma
Lung cancer
Focal segmental glomerulosclerosis
Thrombocytopenia
Hyperkalemia
Stage 5 chronic kidney disease
+16 more conditions
Key Variants
RS1019388756
Conflicting classifications of pathogenicity
Autosomal recessive Alport syndrome, Hematuria, benign familial
Health Risk
RS1026613471
Conflicting classifications of pathogenicity
Autosomal recessive Alport syndrome, COL4A4-related disorder, Alport syndrome
Health Risk
RS1156323870
Conflicting classifications of pathogenicity
Alport syndrome, Autosomal recessive Alport syndrome, Hematuria
Health Risk
RS1158350974
Conflicting classifications of pathogenicity
COL4A4-related disorder, Autosomal recessive Alport syndrome, Hematuria
Health Risk
RS1162654150
Conflicting classifications of pathogenicity
Hematuria, benign familial, 1
Health Risk
RS117468095
Conflicting classifications of pathogenicity
Alport syndrome, Alport syndrome
Health Risk
RS1216718864
Conflicting classifications of pathogenicity
Alport syndrome, Alport syndrome
Health Risk
RS121912863
Conflicting classifications of pathogenicity
Autosomal recessive Alport syndrome, Alport syndrome, Kidney disorder
Health Risk
RS1260916310
Conflicting classifications of pathogenicity
Alport syndrome, Meniere disease, Autosomal recessive Alport syndrome
Health Risk
RS1271416659
Conflicting classifications of pathogenicity
Autosomal dominant Alport syndrome, Autosomal recessive Alport syndrome, Hematuria
Health Risk
RS1287040507
Conflicting classifications of pathogenicity
Hematuria, benign familial, 1
Health Risk
RS13027659
Conflicting classifications of pathogenicity
Alport syndrome, Atypical hemolytic-uremic syndrome, COL4A4-related disorder
Health Risk
All Variants (776)
RSID Category Clinical Significance Conditions
RS1553624127 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1553624173 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Hematuria, benign familial
RS1553627655 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1553639043 Health Risk Likely pathogenic Autosomal dominant Alport syndrome, Autosomal recessive Alport syndrome, Benign familial hematuria
RS1553641728 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Hematuria, benign familial
RS1553644383 Health Risk Likely pathogenic
RS1553646081 Health Risk Likely pathogenic
RS1553681700 Health Risk Likely pathogenic
RS1553681714 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Alport syndrome, Autosomal dominant Alport syndrome
RS1553682895 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Hematuria, benign familial
RS1553683192 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome, Alport syndrome
RS1553688330 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Hematuria, benign familial
RS1553688696 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Hematuria, benign familial
RS1553688712 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1553690604 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1553695389 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Diffuse mesangial sclerosis, Hematuria
RS1553696207 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1553712110 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1559394354 Health Risk Likely pathogenic Autosomal dominant Alport syndrome, Autosomal dominant Alport syndrome
RS1559406956 Health Risk Likely pathogenic
RS1559429663 Health Risk Likely pathogenic
RS1559455617 Health Risk Likely pathogenic Autosomal dominant Alport syndrome, Autosomal dominant Alport syndrome
RS1559515075 Health Risk Likely pathogenic Benign familial hematuria, Autosomal recessive Alport syndrome, Benign familial hematuria
RS1559515185 Health Risk Likely pathogenic
RS1559563141 Health Risk Likely pathogenic Autosomal dominant Alport syndrome, Autosomal dominant Alport syndrome
RS1559563525 Health Risk Likely pathogenic Autosomal dominant Alport syndrome, Benign familial hematuria, Autosomal recessive Alport syndrome
RS1559594442 Health Risk Likely pathogenic Autosomal dominant Alport syndrome, Autosomal recessive Alport syndrome, Benign familial hematuria
RS1559617617 Health Risk Likely pathogenic Alport syndrome, Alport syndrome
RS1559620132 Health Risk Likely pathogenic Autosomal dominant Alport syndrome, Autosomal dominant Alport syndrome
RS1559628183 Health Risk Likely pathogenic Autosomal dominant Alport syndrome, Autosomal dominant Alport syndrome
RS1559643753 Health Risk Likely pathogenic Benign familial hematuria, Benign familial hematuria
RS1559644463 Health Risk Likely pathogenic Autosomal dominant Alport syndrome, Autosomal dominant Alport syndrome
RS1559646395 Health Risk Likely pathogenic Autosomal dominant Alport syndrome, Benign familial hematuria, Autosomal recessive Alport syndrome
RS1575895799 Health Risk Likely pathogenic
RS1576129421 Health Risk Likely pathogenic Autosomal dominant Alport syndrome, Autosomal dominant Alport syndrome
RS1576238292 Health Risk Likely pathogenic
RS1963420059 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1963883799 Health Risk Likely pathogenic
RS1963884904 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1966843131 Health Risk Likely pathogenic
RS1968071233 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1968566020 Health Risk Likely pathogenic COL4A4-related disorder, Autosomal recessive Alport syndrome, Hematuria
RS1968585119 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1968590611 Health Risk Likely pathogenic Hematuria, Autosomal recessive Alport syndrome, Hematuria
RS1968845280 Health Risk Likely pathogenic Benign familial hematuria, Benign familial hematuria
RS1968848668 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1968850188 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1971610561 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1973132502 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS1973140216 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
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