How does the interactive query screen work?
The interactive query page is designed to support manual investigation of specific genes or loci. Simply enter a gene symbol, genomic start / stop position, or probe sequence. Remember to set the radio button to indicate the type of query. The results are displayed on the same page (you may need to scroll down). Each unique splice variant of the gene will be displayed. The variants are identified by accession number and you may click on an accession number to jump to the NCBI transcript record for the variant. Exons are the thick boxes and drawn to scale based on their length. Introns are thin connections between exons and are NOT representative of genomic length. Occasionally small breaks in an exon appear if there is a gap or mismatch of the alignment of the exon to the genome. Dark blue exon sections are coding regions and light blue regions are untranslated regions (3′ and 5′ UTRs). Splice variants drawn in yellow are predicted nonsense mediated decay targets. The last line in the
