![X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failure. - Abstract - Europe PMC X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failure. - Abstract - Europe PMC](https://europepmc.org/articles/PMC3872455/bin/hippokratia-17-211-i001.jpg)
X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failure. - Abstract - Europe PMC
![IJMS | Free Full-Text | Kidney Injury by Variants in the COL4A5 Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental Glomerulosclerosis IJMS | Free Full-Text | Kidney Injury by Variants in the COL4A5 Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental Glomerulosclerosis](https://www.mdpi.com/ijms/ijms-20-00519/article_deploy/html/images/ijms-20-00519-g001.png)
IJMS | Free Full-Text | Kidney Injury by Variants in the COL4A5 Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental Glomerulosclerosis
![Model of the alpha5 chain of type IV collagen and of the COL4A5 gene.... | Download Scientific Diagram Model of the alpha5 chain of type IV collagen and of the COL4A5 gene.... | Download Scientific Diagram](https://www.researchgate.net/publication/21581569/figure/fig1/AS:601798784061448@1520491419458/Model-of-the-alpha5-chain-of-type-IV-collagen-and-of-the-COL4A5-gene-The-deletions-found.png)
Model of the alpha5 chain of type IV collagen and of the COL4A5 gene.... | Download Scientific Diagram
![Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation | Semantic Scholar Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/82dc13ac0ce34674861b1935fc04ef242adaaa56/3-Figure1-1.png)
Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation | Semantic Scholar
![Genotype–phenotype correlation in COL4A3 , COL4A4 and COL4A5 mutations.... | Download Scientific Diagram Genotype–phenotype correlation in COL4A3 , COL4A4 and COL4A5 mutations.... | Download Scientific Diagram](https://www.researchgate.net/publication/8428503/figure/fig1/AS:280798482714628@1443958983817/Genotype-phenotype-correlation-in-COL4A3-COL4A4-and-COL4A5-mutations-XLAS-X-linked.png)
Genotype–phenotype correlation in COL4A3 , COL4A4 and COL4A5 mutations.... | Download Scientific Diagram
![Distribution of small mutations in 30 out of 51 exons of the COL4A5-gene. | Download Scientific Diagram Distribution of small mutations in 30 out of 51 exons of the COL4A5-gene. | Download Scientific Diagram](https://www.researchgate.net/publication/11273052/figure/fig1/AS:601662674710528@1520458968027/Distribution-of-small-mutations-in-30-out-of-51-exons-of-the-COL4A5-gene.png)
Distribution of small mutations in 30 out of 51 exons of the COL4A5-gene. | Download Scientific Diagram
![Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5 | Nature Communications Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5 | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-020-16605-x/MediaObjects/41467_2020_16605_Fig6_HTML.png)
Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5 | Nature Communications
![Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay - Horinouchi - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay - Horinouchi - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/21fb4723-9bc8-4c68-82c7-803f04a4d0cc/mgg31342-fig-0003-m.jpg)
Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay - Horinouchi - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library
![Overview of the COL4A5 mutation identified in Family 3. (A) Pedigree... | Download Scientific Diagram Overview of the COL4A5 mutation identified in Family 3. (A) Pedigree... | Download Scientific Diagram](https://www.researchgate.net/publication/268039064/figure/fig2/AS:273862751420437@1442305376311/Overview-of-the-COL4A5-mutation-identified-in-Family-3-A-Pedigree-for-family-3-A.png)
Overview of the COL4A5 mutation identified in Family 3. (A) Pedigree... | Download Scientific Diagram
![Identification of candidate COL4A5 and COL4A3 variants segregating with... | Download Scientific Diagram Identification of candidate COL4A5 and COL4A3 variants segregating with... | Download Scientific Diagram](https://www.researchgate.net/publication/317292736/figure/fig1/AS:559911767638018@1510504776515/Identification-of-candidate-COL4A5-and-COL4A3-variants-segregating-with-Alport-syndrome.png)
Identification of candidate COL4A5 and COL4A3 variants segregating with... | Download Scientific Diagram
![Mild X-linked Alport syndrome due to the COL4A5 G624D variant originating in the Middle Ages is predominant in Central/East Europe and causes kidney failure in midlife - ScienceDirect Mild X-linked Alport syndrome due to the COL4A5 G624D variant originating in the Middle Ages is predominant in Central/East Europe and causes kidney failure in midlife - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0085253820314101-fx1.jpg)
Mild X-linked Alport syndrome due to the COL4A5 G624D variant originating in the Middle Ages is predominant in Central/East Europe and causes kidney failure in midlife - ScienceDirect
![Fusion of the COL4A5 Gene With NR2F2-AS1 in a Hemangioma Carrying a t(X;15)(q22;q26) Chromosomal Translocation | Cancer Genomics & Proteomics Fusion of the COL4A5 Gene With NR2F2-AS1 in a Hemangioma Carrying a t(X;15)(q22;q26) Chromosomal Translocation | Cancer Genomics & Proteomics](https://cgp.iiarjournals.org/content/cgp/17/4/383/F4.large.jpg)
Fusion of the COL4A5 Gene With NR2F2-AS1 in a Hemangioma Carrying a t(X;15)(q22;q26) Chromosomal Translocation | Cancer Genomics & Proteomics
![Pathogenic Variants in the Genes Affected in Alport Syndrome (COL4A3–COL4A5) and Their Association With Other Kidney Conditions: A Review - American Journal of Kidney Diseases Pathogenic Variants in the Genes Affected in Alport Syndrome (COL4A3–COL4A5) and Their Association With Other Kidney Conditions: A Review - American Journal of Kidney Diseases](https://www.ajkd.org/cms/asset/6f0e562d-00ca-42ec-9131-ae2c71daa3a6/gr1.jpg)
Pathogenic Variants in the Genes Affected in Alport Syndrome (COL4A3–COL4A5) and Their Association With Other Kidney Conditions: A Review - American Journal of Kidney Diseases
![Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis | Journal of Human Genetics Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis | Journal of Human Genetics](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fjhg.2017.28/MediaObjects/10038_2017_Article_BFjhg201728_Fig1_HTML.jpg)