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Homo sapiens Probe hTg737 (polycystic kidney disease, autosomal recessive, in) (TG737), mRNA

NCBI Reference Sequence: NM_006531.1

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    Find regions of similarity between this sequence and other sequences using BLAST.
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    Design and test primers for this sequence using Primer-BLAST.
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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...
  • 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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