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Homo sapiens keratin 10 (KRT10), RefSeqGene on chromosome 17

NCBI Reference Sequence: NG_008405.2

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Reference sequence information

More about the KRT10 gene

Related information

  • Protein
    Protein sequence from Nucleotide coding region
  • Taxonomy
    Taxonomy sequences associated with Nucleotide record
  • Components (Core)
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  • Gene
    Link to related Genes
  • OMIM
    OMIM records associated with Nucleotide sequence
  • PubMed (Weighted)
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  • 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.

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  • Prader-Willi Syndrome
    Prader-Willi Syndrome
    An autosomal dominant disorder caused by deletion of the proximal long arm of the paternal chromosome 15 (15q11-q13) or by inheritance of both of the pair of chromosomes 15 fr...<br/>Year introduced: 1977
    MeSH

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