Homo sapiens complement C1s (C1S), transcript variant 3, mRNA - Nucleotide (original) (raw)
Result Filters
Homo sapiens complement C1s (C1S), transcript variant 3, mRNA
NCBI Reference Sequence: NM_001346850.2
Supplemental Content
Change region shown
Whole sequence
Selected region
from: to:
Customize view
Basic Features
All features
Gene, RNA, and CDS features only
Features added by NCBI
SNP
Display options
Show sequence
Show reverse complement
Show gap features
Analyze this sequence
- Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST. - Pick Primers
Design and test primers for this sequence using Primer-BLAST. - Highlight Sequence Features
Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More... - Find in this Sequence
Finds sub-sequences or patterns in the sequence and highlights the matching regions. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More... - Show in Genome Data Viewer
Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.
Articles about the C1S gene
- Cytoprotective effects of C1s enzyme in macrophages in atherosclerosis mediated through the LRP5 and Wnt/β-catenin pathway. [Mol Immunol. 2024]
Cytoprotective effects of C1s enzyme in macrophages in atherosclerosis mediated through the LRP5 and Wnt/β-catenin pathway.
Mol Immunol. 2024 Feb; 166:29-38. Epub 2024 Jan 12. - A homozygous loss-of-function C1S mutation is associated with Kikuchi-Fujimoto disease. [Clin Immunol. 2023]
A homozygous loss-of-function C1S mutation is associated with Kikuchi-Fujimoto disease.
Alshekaili J, Nasr I, Al-Rawahi M, Ansari Z, Al Rahbi N, Al Balushi H, Al-Zadjali S, Al Kindi M, Al-Maawali A, Cook MC. Clin Immunol. 2023 Jul; 252:109646. Epub 2023 May 18. - Degradation of collagen I by activated C1s in periodontal Ehlers-Danlos Syndrome. [Front Immunol. 2023]
Degradation of collagen I by activated C1s in periodontal Ehlers-Danlos Syndrome.
Amberger A, Pertoll J, Traunfellner P, Kapferer-Seebacher I, Stoiber H, Klimaschewski L, Thielens N, Gaboriaud C, Zschocke J. Front Immunol. 2023; 14:1157421. Epub 2023 Mar 7.
More about the C1S gene
Related information
- Protein
Protein sequence from Nucleotide coding region - PubMed
PubMed articles cited by Nucleotide sequence record - Taxonomy
Taxonomy sequences associated with Nucleotide record - Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes. - BioSystems
BioSystems - CCDS
Link to Consensus CDS - Components (Core)
Links to Core components - Full text in PMC
Free full text articles in PMC - Gene
Link to related Genes - PubMed (RefSeq)
Link to RefSeq PubMed articles - PubMed (Weighted)
Links to pubmed
Recent activity
Finds sub-sequence or patterns in the sequence and highlights the matching region. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences.
More...