Matches in DBpedia 2014 for { <http://dbpedia.org/resource/MEOX2> ?p ?o. }
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- MEOX2 abstract "Homeobox protein MOX-2 is a protein that in humans is encoded by the MEOX2 gene.This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease.".
- MEOX2 entrezgene "4223".
- MEOX2 wikiPageID "14874586".
- MEOX2 wikiPageRevisionID "592472293".
- MEOX2 hasPhotoCollection MEOX2.
- MEOX2 requireManualInspection "no".
- MEOX2 summaryText "This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease.".
- MEOX2 updateCitations "yes".
- MEOX2 updatePage "yes".
- MEOX2 updateProteinBox "yes".
- MEOX2 updateSummary "yes".
- MEOX2 subject Category:Transcription_factors.
- MEOX2 type Biomolecule.
- MEOX2 type Protein.
- MEOX2 type BiologicalObject.
- MEOX2 comment "Homeobox protein MOX-2 is a protein that in humans is encoded by the MEOX2 gene.This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease.".
- MEOX2 label "MEOX2".
- MEOX2 sameAs m.03g_tj5.
- MEOX2 sameAs Q15996792.
- MEOX2 sameAs Q15996792.
- MEOX2 wasDerivedFrom MEOX2?oldid=592472293.
- MEOX2 isPrimaryTopicOf MEOX2.