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Homo sapiens mutS homolog 2 (MSH2), transcript variant 8, mRNA

NCBI Reference Sequence: NM_001406636.1

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    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...
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    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.

Reference sequence information

  • RefSeq protein product
    See the reference protein sequence for DNA mismatch repair protein Msh2 isoform 8 (NP_001393565.1).

More about the MSH2 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
  • Components (Core)
    Links to Core components
  • Gene
    Link to related Genes
  • OMIM
    OMIM records associated with Nucleotide sequence
  • PubMed (RefSeq)
    Link to RefSeq PubMed articles
  • PubMed (Weighted)
    Links to pubmed

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