Mar 5, 2021 GeneCards Summary for CTSS Gene. CTSS (Cathepsin S) is a Protein Coding gene. Diseases associated with CTSS include Dacryoadenitis
Biological context of CTSS. 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.
Among its related pathways are Bacterial infections in CF airways and Degradation of the extracellular matrix . 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 … 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. Thiol protease.
Variants classified as unknown significance (VUS), likely pathogenic, or pathogenic will be reported. Cystinosis. More than 80 different mutations that are responsible for causing cystinosis have been identified in the CTNS gene. The most common mutation is a deletion of a large part of the CTNS gene (sometimes referred to as the 57-kb deletion), resulting in the complete loss of cystinosin.
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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.
Thiol protease. Key protease responsible for the removal of the invariant chain from MHC class II molecules and MHC class II antigen presentation. The bond-specificity of this proteinase is in part similar to the specificities of cathepsin L.
Nth. Tidigare Student vid Qifa Primary School. 1 januari 2010 - 21 november 2014. Högskola/ The expression levels of four genes identified by microarray screening (PLCB2, HVCN1, CTSS, and DEF8) and one purine/thiopurine related gene (NME6) Cap analys av Gene Expression (CAGE) är en metod för genombred av ROC kurvor visar att SLIC-CAGE kraftigt överträffar nanoCAGE i CTSS identifiering. och CTSS) samtidigt som antiinflammatoriska IL-33 hade nedreglerats. Cobra completes MCB for CombiGene's gene therapy candidate.
Variants classified as unknown significance (VUS), likely pathogenic, or pathogenic will be reported.
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1 januari 2010 - 21 november 2014. Högskola/ The expression levels of four genes identified by microarray screening (PLCB2, HVCN1, CTSS, and DEF8) and one purine/thiopurine related gene (NME6) Cap analys av Gene Expression (CAGE) är en metod för genombred av ROC kurvor visar att SLIC-CAGE kraftigt överträffar nanoCAGE i CTSS identifiering. och CTSS) samtidigt som antiinflammatoriska IL-33 hade nedreglerats. Cobra completes MCB for CombiGene's gene therapy candidate.
CTSS : Synonyms. Description.
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Tidigt 60-tal: CTSS, tidig tidsdelning och Project MAC Det är välkänt att Gene Amdahl , en viktig FS-spelare, fortsatte att sträva efter FS-mål
1520 cathepsin S. 1. 150702672. 150738433 -. -0,145.
CTSS (cathepsin S) is a protein-coding gene. Diseases associated with CTSS include cercarial dermatitis, and abdominal aortic aneurysm. GO annotations related to this gene include cysteine-type endopeptidase activity. An important paralog of this gene is CTSF.
. The mature protein cleaves the invariant CTSS (cathepsin S), Authors: Dessen P. Published in: Atlas Genet Cytogenet Oncol Haematol.
It's used to fix, turn off or add genes to your genetic code. 2011-04-01 · The following TaqMan Gene Expression Assays (Applied Biosystems, Foster City, CA, USA) were used for cDNA transcript quantification: Hs00374176_m1 for CD40 (exon boundary 1–2, amplicon length 101), Hs00175403_m1 for CTSS (exon boundary 3–4, amplicon length 82), Hs00947433_m1 for CTSB (exon boundary 2–3, amplicon length 73), and Human PPIA (cyclophilin A) Endogenous Control (4326316E) as UCSC Genes CTSS (uc001evn.3) at chr1:150702672-150738433 - Homo sapiens cathepsin S (CTSS), transcript variant 1, mRNA.