Matches in SemOpenAlex for { <https://semopenalex.org/work/W2545015629> ?p ?o ?g. }
- W2545015629 endingPage "44" @default.
- W2545015629 startingPage "29" @default.
- W2545015629 abstract "COL4A1 and COL4A2 are extracellular matrix proteins that form heterotrimers and are present in nearly all basement membranes in every organ. In the past decade, COL4A1 and COL4A2 mutations have been identified to cause a multi-system disorder for which penetrance and severity of constituent phenotypes can greatly vary. Here, we compare the outcomes of more than 100 mutations identified in patients and data from a murine allelic series to explore the presence of genotype–phenotype correlations – many of which are shared among other types of collagen. We find that there is a frequency bias for COL4A1 over COL4A2 mutations and that glycine (Gly) substitutions within the triple helical domain are the most common class of mutations. Glycine is most often replaced by a charged amino acid, however the position of the mutation, and not the properties of the substituting amino acid, appears to have a greater influence on disease severity. Moreover, the impact of position is not straightforward. Observations from a murine allelic series suggest that mutations in the NC1 domain may result in relatively mild phenotypes via a ‘quantitative’ mechanism similar to other types of collagens, however, this effect was not apparent in human reports. Importantly, other position-dependent effects had differential impacts depending on the phenotype of interest. For example, the severity of cerebrovascular disease correlated with an amino-to-carboxy severity gradient for triple-helical glycine substitutions whereas the penetrance and severity of myopathy and nephropathy appear to involve a functional sub-domain(s). Greater understanding of genotype–phenotype correlations and the interaction of consequences of different mutations will be important for patient prognosis and care and for developing mechanism-based therapeutics to treat individual components of this emerging syndrome." @default.
- W2545015629 created "2016-11-04" @default.
- W2545015629 creator A5062427842 @default.
- W2545015629 creator A5076132705 @default.
- W2545015629 date "2017-01-01" @default.
- W2545015629 modified "2023-10-16" @default.
- W2545015629 title "Genotype-phenotype correlations in pathology caused by collagen type IV alpha 1 and 2 mutations" @default.
- W2545015629 cites W140794799 @default.
- W2545015629 cites W1483387915 @default.
- W2545015629 cites W1502624346 @default.
- W2545015629 cites W1521876081 @default.
- W2545015629 cites W1536187379 @default.
- W2545015629 cites W1579446540 @default.
- W2545015629 cites W1593898347 @default.
- W2545015629 cites W170942874 @default.
- W2545015629 cites W1835593276 @default.
- W2545015629 cites W1849608740 @default.
- W2545015629 cites W1886835423 @default.
- W2545015629 cites W1959029222 @default.
- W2545015629 cites W1964196602 @default.
- W2545015629 cites W1964515302 @default.
- W2545015629 cites W1964849358 @default.
- W2545015629 cites W1970298553 @default.
- W2545015629 cites W1975257902 @default.
- W2545015629 cites W1977150529 @default.
- W2545015629 cites W1978486342 @default.
- W2545015629 cites W1983321321 @default.
- W2545015629 cites W1989736688 @default.
- W2545015629 cites W1990461954 @default.
- W2545015629 cites W1992025623 @default.
- W2545015629 cites W1996530196 @default.
- W2545015629 cites W1998998498 @default.
- W2545015629 cites W1999190014 @default.
- W2545015629 cites W2000058971 @default.
- W2545015629 cites W2000382581 @default.
- W2545015629 cites W2001512757 @default.
- W2545015629 cites W2002356328 @default.
- W2545015629 cites W2006505323 @default.
- W2545015629 cites W2008400639 @default.
- W2545015629 cites W2011472454 @default.
- W2545015629 cites W2013383208 @default.
- W2545015629 cites W2014832158 @default.
- W2545015629 cites W2017126456 @default.
- W2545015629 cites W2020648421 @default.
- W2545015629 cites W2020816917 @default.
- W2545015629 cites W2023371427 @default.
- W2545015629 cites W2026542895 @default.
- W2545015629 cites W2029769832 @default.
- W2545015629 cites W2029863361 @default.
- W2545015629 cites W2030732677 @default.
- W2545015629 cites W2030840013 @default.
- W2545015629 cites W2031805491 @default.
- W2545015629 cites W2032756767 @default.
- W2545015629 cites W2032783021 @default.
- W2545015629 cites W2044528429 @default.
- W2545015629 cites W2049440576 @default.
- W2545015629 cites W2051136095 @default.
- W2545015629 cites W2053895193 @default.
- W2545015629 cites W2057831089 @default.
- W2545015629 cites W2059230482 @default.
- W2545015629 cites W2059684463 @default.
- W2545015629 cites W2060618525 @default.
- W2545015629 cites W2061303238 @default.
- W2545015629 cites W2065418557 @default.
- W2545015629 cites W2069566684 @default.
- W2545015629 cites W2070273704 @default.
- W2545015629 cites W2082432121 @default.
- W2545015629 cites W2086949096 @default.
- W2545015629 cites W2095212078 @default.
- W2545015629 cites W2096252197 @default.
- W2545015629 cites W2096500584 @default.
- W2545015629 cites W2098001302 @default.
- W2545015629 cites W2100297351 @default.
- W2545015629 cites W2101044183 @default.
- W2545015629 cites W2103188558 @default.
- W2545015629 cites W2110309692 @default.
- W2545015629 cites W2110921813 @default.
- W2545015629 cites W2113869585 @default.
- W2545015629 cites W2114368562 @default.
- W2545015629 cites W2115536425 @default.
- W2545015629 cites W2121655734 @default.
- W2545015629 cites W2123872376 @default.
- W2545015629 cites W2125903388 @default.
- W2545015629 cites W2126255082 @default.
- W2545015629 cites W2126756606 @default.
- W2545015629 cites W2127923616 @default.
- W2545015629 cites W2128796050 @default.
- W2545015629 cites W2134144117 @default.
- W2545015629 cites W2135329373 @default.
- W2545015629 cites W2142301722 @default.
- W2545015629 cites W2143156113 @default.
- W2545015629 cites W2145869447 @default.
- W2545015629 cites W2146260953 @default.
- W2545015629 cites W2150204018 @default.
- W2545015629 cites W2152114747 @default.
- W2545015629 cites W2153216732 @default.
- W2545015629 cites W2157592619 @default.
- W2545015629 cites W2159470215 @default.