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C1orf167

WebMar 29, 2024 · C1orf167 chromosome 1 open reading frame 167 [ (human)] Gene ID: 284498, updated on 4-Nov-2024 Summary Implicated in coronary artery disease. … WebThe .gov means it's official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.

C1orf167 protein expression summary - The Human …

WebOct 11, 2024 · The frequency of the homozygote C677T genotype showed an inverse-U-shaped geospatial pattern globally with a pronounced frequency in northern China, which coincided with the high prevalence of hyperhomocysteinemia (HHCY) in northern China. WebEstablished in 1937, Mopar is the official service, parts, and customer care provider for Fiat Chrysler Automobiles (FCA). Every Mopar part guarantees factory-authorized … medical term shin https://dreamsvacationtours.net

MTHFR Mutation. Phoenix Rising ME/CFS Forums

WebMar 5, 2024 · Description: single nucleotide variant Variant details Conditions Gene (s) Help NM_001010881.2 (C1orf167):c.3924C>T (p.His1308=) Allele ID 276682 Variant type single nucleotide variant Variant length 1 bp Cytogenetic location 1p36.22 Genomic location 1: 11788224 (GRCh38) GRCh38 UCSC 1: 11848281 (GRCh37) GRCh37 UCSC HGVS ... WebMar 13, 2024 · Mopar Replacement Crankshaft Position Sensors 5149167AF. Write the First Review. Part Number: MOP-05149167AF. $19.99. Mopar Replacement Crankshaft … WebC1orf167 Gene - Somatic Mutations in Cancer Gene GRCh38 · COSMIC v97 Gene view The gene view histogram is a graphical view of mutations across C1ORF167. These … light shop opinie

C1orf167 Gene - Somatic Mutations in Cancer - Wellcome Sanger …

Category:Frontiers Exome-Wide Association Study Identifies East Asian …

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C1orf167

C1orf167 antibody Immunohistochemistry HPA039114 - Sigma-Aldrich

Chromosome 1 open reading frame (C1orf167) is a protein which in humans is encoded by the C1orf167 gene. The NCBI accession number is NP_001010881. The protein is 1468 amino acids in length with a molecular weight of 162.42 kDa. The mRNA sequence was found to be 4689 base pairs in length. WebPharos is the web interface for data collected by the Illuminating the Druggable Genome initiative. Target, disease and ligand information are collected and displayed.

C1orf167

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WebHuman Gene C1orf167 (ENST00000433342.6) from GENCODE V43 Description: Event=Alternative splicing; Named isoforms=2; Name=1; IsoId=Q5SNV9-1; Sequence=Displayed; Name=2; IsoId=Q5SNV9-2; Sequence=VSP_028420; Note=No experimental confirmation available; (from UniProt Q5SNV9) Gencode Transcript: … WebSnp C1orf167 C 1202883 20, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, …

Web(Click on the icon in the table below to see search hit context) WebPolydactyly is a rare autosomal dominant or recessive appendicular patterning defect of the hands and feet, phenotypically characterized by the duplication of digits. Postaxial polydactyly (PAP) is the most common form and includes two main types: PAP type A (PAPA) and PAP type B (PAPB). Type A involves a well-established extra digit …

WebC1orf167 - chromosome 1 open reading frame 167 Gene. Gene. Protein. Ortholog. Homo sapiens. Gene ID: 284498 Gene type: protein coding. About C1orf167. This gene has 8 transcripts (splice variants) and 30 orthologues. Broad expression in testis (RPKM 7.7), lung (RPKM 3.1) and 24 other tissues. WebC1orf167 - chromosome 1 open reading frame 167 There are no transcripts associated with this gene. CLCN6 - chloride voltage-gated channel 6 There are no transcripts associated with this gene. Back To Top More Information Set Membership: HapMap JSNP Panther Classification: Molecular Function -

WebNot detected in human brain. Single cell type specificityi. The RNA specificity category is based on mRNA expression levels in the analyzed cell types based on scRNA-seq data …

Web2011-2024 Mopar part # 05149167AF - Crankshaft Position Sensor from WeRMopar, the leader in online MoparParts. medical term shiny skinWebDESCRIPTION: RecName: Full=Uncharacterized protein C1orf167; SEQUENCE CAUTION: Sequence=CAI15881.1; Type=Erroneous gene model prediction; Primer design for this transcript : Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA. light shop penrithWebHPA039114 Anti-C1orf167 antibody produced in rabbit (0) Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution Synonym (s): Anti-DKFZp434E1410, Anti-RP11-56N19.2, Anti-Uncharacterized protein C1orf167 Human Protein Atlas Number: HPA039114 Pricing and availability is not … light shop perthWebMar 29, 2024 · C1orf167. chromosome 1 open reading frame 167. Gene ID: 284498, updated on 4-Nov-2024. Gene type: protein coding. See all available tests in GTR for … medical term shinglesWebPrEST Antigen C1orf167 [Catalog No.: ATL-APrEST77100] Toggle menu. Compare ; Phone: 760-431-4600 / Fax: 760-431-4604; Sign in or Register; Cart 0. Search. CURRENT PROMOTIONS. WORLDWIDE DISTRIBUTION. CONTACT US. Neurodegeneration Products; CUSABIO dashboard; Fukushima Cancer Gene Overexpressing Cell Lines; medical term shin boneWeb【质控标准】 1. 阴性质控品的检测结果应为阴性,无指数扩增期,Ct=40或无Ct; 2. 阳性质控品的检测结果应为阳性,有明显的指数扩增期,Ct值应小于等于35; light shop orpingtonWebA pathway analysis online textbook: Workflows provide step-by-step instruction to pathway analysis; primers for deep-dives into concepts. Data File Downloads Data prepared in a variety of formats including Biological Pathway Exchange (BioPAX), Simple Interaction Format (sif) and as a Gene Set Database (gmt). Available per datasource. light shop ormond