chickvasup.blogg.se

Sequence chromatogram viewer
Sequence chromatogram viewer







  1. SEQUENCE CHROMATOGRAM VIEWER HOW TO
  2. SEQUENCE CHROMATOGRAM VIEWER SKIN

Status: VALIDATED Description Transcript Variant: This variant (2) lacks an alternate in-frame exon in the coding region, compared to variant 1. NM_001289403.2 → NP_001276332.1 MMS19 nucleotide excision repair protein homolog isoform 2 This section to the one reported in Genomic regions, Identify version mismatches by comparing the version of the RefSeq in These reference sequences are curated independently of the genomeĪnnotation cycle, so their versions may not match the RefSeq versions in the current These reference sequences exist independently of genome builds. See citations in PubMed for homologs of this gene provided by HomoloGene

  • Predictive impact of common variations in DNA repair genes on clinical outcome of osteosarcoma.
  • Cancer Epidemiol Biomarkers Prev, 2009 Apr.
  • Nucleotide excision repair pathway polymorphisms and pancreatic cancer risk: evidence for role of MMS19L.
  • Methyl-methanesulfonate sensitivity 19 expression is associated with metastasis and chemoradiotherapy response in esophageal cancer.
  • MMS19 as a potential predictive marker of adjuvant chemotherapy benefit in resected non-small cell lung cancer.
  • MMS19 localizes to mitochondria and protects the mitochondrial genome from oxidative damage.
  • SEQUENCE CHROMATOGRAM VIEWER SKIN

    Expression Ubiquitous expression in testis (RPKM 18.2), skin (RPKM 14.7) and 25 other tissues See more Orthologs mouse all NEW Try the new Gene table Located in cytosol nucleoplasm and spindle. Involved in several processes, including iron-sulfur cluster assembly positive regulation of nucleobase-containing compound metabolic process and protein maturation by iron-sulfur cluster transfer. Database of Single Nucleotide Polymorphisms (dbSNP)įull Name MMS19 homolog, cytosolic iron-sulfur assembly component provided by HGNC Primary source HGNC:HGNC:13824 See related Ensembl:ENSG00000155229 MIM:614777 AllianceGenome:HGNC:13824 Gene type protein coding RefSeq status VALIDATED Organism Homo sapiens Lineage Eukaryota Metazoa Chordata Craniata Vertebrata Euteleostomi Mammalia Eutheria Euarchontoglires Primates Haplorrhini Catarrhini Hominidae Homo Also known as CIAO4 MET18 MMS19L hMMS19 Summary Enables estrogen receptor binding activity and transcription coactivator activity.Database of Genomic Structural Variation (dbVar).Online Mendelian Inheritance in Man (OMIM).Database of Genotypes and Phenotypes (dbGaP).Structure (Molecular Modeling Database).Conserved Domain Search Service (CD Search).BLAST (Basic Local Alignment Search Tool).

    SEQUENCE CHROMATOGRAM VIEWER HOW TO

    View the visual guide for changing Windows file associations for more information about how to change file associations in Windows. Choose an icon to replace the missing icon, click OK, and restart your computer.Click OK, then Change Icon, then Browse.Type "Folders" in the Application box, and "AppProperties" in the Topics box.Click the Use DDE check box and type "" in the DDE Message box.Type "Open" in the Action box, and type "c:\progra~1\intern~1\iexplore.exe" in the Application Used To Perform Action box.Type "Windows Explorer Command" in the Description Of Type box and click New.Select "SimTown Sounds" within the Registered File Types box and click Edit.Select "Folder Options" from the View menu in an open window and then click the File Types tab.To change the SCF file extension back to the default Windows association, follow these steps (provided by Microsoft): NOTE: SimTown may alter the standard SCF file association in Windows and cause the "Show Desktop" and "View Channels" icons in the Task Bar to change.









    Sequence chromatogram viewer