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
RS2150773718 Health Risk Likely pathogenic
RS2150794687 Health Risk Likely pathogenic
RS2150805752 Health Risk Likely pathogenic
RS2150877933 Health Risk Likely pathogenic Benign familial hematuria, Benign familial hematuria
RS2472735253 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2472735627 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473003981 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473005339 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473008834 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473010935 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Hematuria, benign familial
RS2473119530 Health Risk Likely pathogenic
RS2473342112 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473343738 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473355271 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473357313 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473357970 Health Risk Likely pathogenic
RS2473400519 Health Risk Likely pathogenic COL4A4-related disorder, COL4A4-related disorder
RS2473691099 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473692907 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473693902 Health Risk Likely pathogenic
RS2473714807 Health Risk Likely pathogenic Autosomal dominant Alport syndrome, Autosomal dominant Alport syndrome
RS2473720581 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473863644 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473864066 Health Risk Likely pathogenic
RS2473864723 Health Risk Likely pathogenic COL4A4-related disorder, Autosomal recessive Alport syndrome, COL4A4-related disorder
RS2473865757 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473939208 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473939660 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473939910 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Hematuria, benign familial
RS2473967532 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473967848 Health Risk Likely pathogenic
RS2473972925 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2473974398 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2474010076 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2474010597 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2474012131 Health Risk Likely pathogenic
RS2474078466 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2474115806 Health Risk Likely pathogenic
RS2474116506 Health Risk Likely pathogenic
RS2474116574 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2474117368 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2474117528 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2474118082 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2474160561 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Hematuria, benign familial
RS2474161328 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2474215752 Health Risk Likely pathogenic Benign familial hematuria, Autosomal recessive Alport syndrome, Hematuria
RS2474218124 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2474220383 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
RS2474221510 Health Risk Likely pathogenic Hematuria, benign familial, 1
RS2474222643 Health Risk Likely pathogenic Autosomal recessive Alport syndrome, Autosomal recessive Alport syndrome
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