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PREDICTED: Homo sapiens solute carrier family 2 member 12 (SLC2A12), transcript variant X3, mRNA

NCBI Reference Sequence: XM_054354351.1

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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...
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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...
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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 alternative splicing
    See 5 reference mRNA sequence splice variants for the SLC2A12 gene.
  • RefSeq protein product
    See the reference protein sequence for solute carrier family 2, facilitated glucose transporter member 12 isoform X1 (XP_054210326.1).

More about the SLC2A12 gene

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