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- HEXA abstract "Hexosaminidase A (alpha polypeptide), also known as HEXA, is an enzyme that in humans is encoded by the HEXA gene, located on the 15th chromosome.Hexosaminidase A and the cofactor GM2 activator protein catalyze the degradation of the GM2 gangliosides and other molecules containing terminal N-acetyl hexosamines. Hexosaminidase A is a heterodimer composed of an alpha subunit (this protein) and a beta subunit. The alpha subunit polypeptide is encoded by the HEXA gene while the beta subunit is encoded by the HEXB gene. Gene mutations in the gene encoding the beta subunit (HEXB) often result in Sandhoff disease; whereas, mutations in the gene encoding the alpha subunit (HEXA, this gene) decrease the hydrolysis of GM2 gangliosides, which is the main cause of Tay–Sachs disease.".
- HEXA entrezgene "3073".
- HEXA thumbnail HEXA_location.png?width=300.
- HEXA wikiPageExternalLink taysachs.php.
- HEXA wikiPageID "14303889".
- HEXA wikiPageLength "12373".
- HEXA wikiPageOutDegree "23".
- HEXA wikiPageRevisionID "678842204".
- HEXA wikiPageWikiLink Arginine.
- HEXA wikiPageWikiLink Category:Genes_on_human_chromosome_15.
- HEXA wikiPageWikiLink Chromosome_15_(human).
- HEXA wikiPageWikiLink Codon.
- HEXA wikiPageWikiLink Enzyme.
- HEXA wikiPageWikiLink GM2A.
- HEXA wikiPageWikiLink Ganglioside.
- HEXA wikiPageWikiLink Gangliosides.
- HEXA wikiPageWikiLink Gene.
- HEXA wikiPageWikiLink Genetic_code.
- HEXA wikiPageWikiLink Glutamic_acid.
- HEXA wikiPageWikiLink Glycine.
- HEXA wikiPageWikiLink HEXB.
- HEXA wikiPageWikiLink Heterodimer.
- HEXA wikiPageWikiLink Hexosaminidase.
- HEXA wikiPageWikiLink Hydrolysis.
- HEXA wikiPageWikiLink Hydrolyze.
- HEXA wikiPageWikiLink Mutation.
- HEXA wikiPageWikiLink Mutations.
- HEXA wikiPageWikiLink Pneumonia.
- HEXA wikiPageWikiLink Proline.
- HEXA wikiPageWikiLink Protein_dimer.
- HEXA wikiPageWikiLink Sandhoff_disease.
- HEXA wikiPageWikiLink Serine.
- HEXA wikiPageWikiLink Tay–Sachs_disease.
- HEXA wikiPageWikiLink File:HEXA_location.png.
- HEXA wikiPageWikiLinkText "HEXA".
- HEXA wikiPageWikiLinkText "hexosaminidase A".
- HEXA wikiPageWikiLinkText "β-hexosaminidase A".
- HEXA hasPhotoCollection HEXA.
- HEXA requireManualInspection "no".
- HEXA updateCitations "yes".
- HEXA updatePage "yes".
- HEXA updateProteinBox "yes".
- HEXA updateSummary "no".
- HEXA wikiPageUsesTemplate Template:Commons_category.
- HEXA wikiPageUsesTemplate Template:EC_number.
- HEXA wikiPageUsesTemplate sphingolipid_metabolism_enzymes.
- HEXA wikiPageUsesTemplate Template:MeshName.
- HEXA wikiPageUsesTemplate Template:PBB.
- HEXA wikiPageUsesTemplate Template:PBB_Controls.
- HEXA wikiPageUsesTemplate Template:PBB_Further_reading.
- HEXA wikiPageUsesTemplate Template:PDB_Gallery.
- HEXA wikiPageUsesTemplate Template:Refbegin.
- HEXA wikiPageUsesTemplate Template:Refend.
- HEXA wikiPageUsesTemplate Template:Reflist.
- HEXA wikiPageUsesTemplate Template:Sugar_hydrolases.
- HEXA subject Category:Genes_on_human_chromosome_15.
- HEXA hypernym Enzyme.
- HEXA type Biomolecule.
- HEXA type Protein.
- HEXA type Thing.
- HEXA type Q206229.
- HEXA type Q8054.
- HEXA comment "Hexosaminidase A (alpha polypeptide), also known as HEXA, is an enzyme that in humans is encoded by the HEXA gene, located on the 15th chromosome.Hexosaminidase A and the cofactor GM2 activator protein catalyze the degradation of the GM2 gangliosides and other molecules containing terminal N-acetyl hexosamines. Hexosaminidase A is a heterodimer composed of an alpha subunit (this protein) and a beta subunit.".
- HEXA label "HEXA".
- HEXA sameAs Category:HEXA.
- HEXA sameAs m.03c_zns.
- HEXA sameAs Q5629495.
- HEXA sameAs Q5629495.
- HEXA wasDerivedFrom HEXA?oldid=678842204.
- HEXA depiction HEXA_location.png.
- HEXA isPrimaryTopicOf HEXA.