Results of annotation for all analyses with previously reported candidate genes, QTL or association in SNP region.Sarah, BergfelderDrüingChristine, GroßeBrinkhausBianca, LindMalena, ErbeKarl, SchellanderHenner, SimianerErnst, Tholen
descendants of several chromosomal elements have two alpha chromosomes in gar and Australian lungfish but only one clear alpha chromosome remains in South American and African lungfish (with the alpha copies having lost genes). Retention rates were computed as the percentage of the retained (present)...
Group I introns are a distinct class of RNA self-splicing introns with an ancient origin. All known group I introns present in eukaryote nuclei interrupt functional ribosomal RNA genes located in ribosomal DNA... Authors: Annica Hedberg and Steinar D Johansen Citation: Mobile DNA 2013 4:17 ...
In addition, the seventh site inTable 2, cg10589813, replicates in LBC and is supported by SATSA. It is located in the south shore of a CpG island, which lies near theCEBPBgene, encoding an important transcription factor involved in the regulation of the expression of genes involved in immu...
Methods: While several publications have made use of the metabolites and metabolic pathways available in the Kyoto Encyclopedia of Genes and Genomes (KEGG), we downloaded all the compound entries with pathway annotations available in the KEGG. From these data, we constructed a dataset where each ...
(whole genome, high-confidence calling, repetitive, GC content of >0.85, GC content of <0.15, low mappability, the ACMG59 genes and regions of large duplications (>1 kb)). Using random batches as a control set, all comparisons had a Cohen’sdof <0.35. Here we report any Cohen’sd...
A total of 689 gene variants, involving 308 genes, met those criteria. These genes were then categorized by GAD-Disease using the Functional Annotation tools from the Database for Annotation, Visualization and Integrated Discovery (DAVID) Bioinformatics Resources 6.8 (https://david.ncifcrf.gov/) ...
pathway by promoting specific molecules in the normal pathways that may have been affected in the diseased state. In addition, these drugs should also be designed so as not to affect any other important “off-target” molecules or antitargets that may be similar in appearance to the target ...
22q11.2 deletion syndrome (22q11DS), a copy number variation (CNV) disorder, occurs in approximately 1:4000 live births due to a heterozygous microdeletion at position 11.2 (proximal) on the q arm of human chromosome 22 (hChr22) (McDonald-McGinn and Sull
the Trehalose Phosphorylase pathway, for which putative genes have been identified and partially characterized in N. crassa[40] and A. fumigatus[22] and also exist in A. niger (ANI_1_2720024). However, it is possible to generate mutants, within the homologous Tps/Tpp group, in A. ...