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Homo sapiens imprinted in Prader-Willi syndrome (IPW), RefSeqGene on chromosome 15

NCBI Reference Sequence: NG_021193.1

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    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...
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    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...

More about the IPW gene

Related information

  • PubMed
    PubMed articles cited by Nucleotide sequence record
  • Taxonomy
    Taxonomy sequences associated with Nucleotide record
  • Components (Core)
    Links to Core components
  • Full text in PMC
    Free full text articles in PMC
  • Gene
    Link to related Genes
  • OMIM
    OMIM records associated with Nucleotide sequence
  • RNA
    RNA sequence records that are annotated on the current genomic nucleotide sequences. The RNA records represent aligned or predicted transcripts of the current records.
  • SNP
    Related SNPs

LinkOut to external resources

  • reagents [ExactAntigen/Labome]
    reagents
    ExactAntigen/Labome

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