The gene view histogram is a graphical view of mutations across CTSS. These mutations are displayed at the amino acid level across the full length of the gene by default. Restrict the view to a region of the gene by dragging across the histogram to highlight the region of interest, or by using the sliders in the filters panel to the left.

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Gene: Ctss ENSMUSG00000038642 Gene Synonyms. Cat S. Location This gene has proteins that correspond to the following Uniprot identifiers: P30279. May 12, 2020 CTSS production, activation, and secretion. The Ctss gene is found at the 1q21 chromosome in humans and, like all lysosomal cathepsins, is Using the breast cancer dataset, survival dependent on CTSS gene expression was analysed based on intrinsic patient subtype, using a collation of previously CTSS (cathepsin S) · Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, go to How to contribute Jan 29, 2020 Gene expression of Ctss, together with the pro-inflammatory cytokines, Ifng and Tnf, were significantly elevated in NOD mouse LG (Fig. 2A) Mar 1, 2000 We found a novel G → A change at nucleotide −25 within the promoter of the CTSS gene encoding the elastase cathepsin S. The Apr 23, 2020 kine perturbation. Human FL Biopsy Samples with CTSS Y132 Mutations.

Ctss gene

The frequency of the CTSS-25A allele was 0.457 in Caucasians and 0.431 in Canadian Inuit. Because of the importance of the CTSS gene product in vascular matrix remodeling, this polymorphism may be useful in the study of associations with atherosclerosis and related phenotypes. To examine the functional ramifications associated with greater Ctss expression, the Ctss gene was deleted in the mdx genetic background, resulting in protection from muscular dystrophy pathogenesis that included reduced myofiber turnover and histopathology, reduced fibrosis, and improved running capacity. CTSS has 5,430 functional associations with biological entities spanning 8 categories (molecular profile, organism, chemical, functional term, phrase or reference, disease, phenotype or trait, structural feature, cell line, cell type or tissue, gene, protein or microRNA) extracted from 78 datasets.

These mutations are displayed at the amino acid level across the full length of the gene by default. Restrict the view to a region of the gene by dragging across the histogram to highlight the region of interest, or by using the sliders in the filters panel to the left.

2020-07-01

2 RefSeqs (NM) Availability. Made to Order. Catalog # A15629, A15630 Non-tailed | Desalted | Pair : See in cart, See in cart Add Pair To Cart Add to Array View Description: Homo sapiens cathepsin S (CTSS), transcript variant 1, mRNA.

Mar 1, 2000 We found a novel G → A change at nucleotide −25 within the promoter of the CTSS gene encoding the elastase cathepsin S. The

Conclusion: The single nucleotide polymorphisms (SNPs) of rs774320676 and rs928508030 of CTSS gene were related with risk for acute atherosclerotic cerebral infarction. The T allele at rs774320676 locus and G allele at rs928508030 locus of CTSS were genetic susceptibility genes of acute atherosclerotic cerebral infarction. 2020-04-09 · Moreover, Gene Set Enrichment Analysis (GSEA) was also employed, which indicated that LRFI chickens increased expression of genes related to mitochondrial function. Furthermore, protein network interaction and function analyses revealed ND2, ND4, CYTB, RAC2, VCAM1, CTSS and TLR4 were key genes for feed efficiency. The protein CTSS, a member of the peptidase C1 family, is a lysosomal cysteine proteinase that may participate in the The following CTSS gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the CTSS cDNA ORF which is encoded by the open reading frame (ORF) sequence.

Overall reliability score for the subcellular location (s) of the protein (s) in human cells, and summary of the antibodies used for immunostainings. Read more. Reliability scorei. Overall gene reliability score for the subcellular location (s) of the encoded protein (s). CTSS has 5,430 functional associations with biological entities spanning 8 categories (molecular profile, organism, chemical, functional term, phrase or reference, disease, phenotype or trait, structural feature, cell line, cell type or tissue, gene, protein or microRNA) extracted from 78 datasets. Ctss Gene Detail Summary Symbol. Ctss Name.
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Diseases associated with CTSC include Papillon-Lefevre Syndrome and Haim-Munk Syndrome.

Gene descriptioni.
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3.570971 3.557132 3.297147 3.504174 3.130115 3.126201 3.326192 3.546335 3.645422 3.179926 3.194895 3.543543 2434575 "CTSS" 4.77645 4.816613

Preliminary data : if you are an author who wish to write a full paper/card on this gene, go to How to contribute Jan 29, 2020 Gene expression of Ctss, together with the pro-inflammatory cytokines, Ifng and Tnf, were significantly elevated in NOD mouse LG (Fig.