Matches in DBpedia 2014 for { <http://dbpedia.org/resource/LAT2> ?p ?o. }
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- LAT2 abstract "Linker for activation of T-cells family member 2 is a protein that in humans is encoded by the LAT2 gene.This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein.".
- LAT2 entrezgene "7462".
- LAT2 wikiPageID "14778042".
- LAT2 wikiPageRevisionID "592157226".
- LAT2 hasPhotoCollection LAT2.
- LAT2 requireManualInspection "no".
- LAT2 summaryText "This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein.".
- LAT2 updateCitations "yes".
- LAT2 updatePage "yes".
- LAT2 updateProteinBox "yes".
- LAT2 updateSummary "yes".
- LAT2 type Biomolecule.
- LAT2 type Protein.
- LAT2 type BiologicalObject.
- LAT2 comment "Linker for activation of T-cells family member 2 is a protein that in humans is encoded by the LAT2 gene.This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein.".
- LAT2 label "LAT2".
- LAT2 sameAs m.03gxqdm.
- LAT2 sameAs Q6457131.
- LAT2 sameAs Q6457131.
- LAT2 wasDerivedFrom LAT2?oldid=592157226.
- LAT2 isPrimaryTopicOf LAT2.