Matches in DBpedia 2014 for { <http://dbpedia.org/resource/ERCC5> ?p ?o. }
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- ERCC5 abstract "DNA repair protein complementing XP-G cells is a protein that in humans is encoded by the ERCC5 gene.Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Multiple alternatively spliced transcript variants encoding distinct isoforms have been described, but the biological validity of all variants has not been determined.Mutations in ERCC5 cause arthrogryposis .".
- ERCC5 entrezgene "2073".
- ERCC5 wikiPageExternalLink br.fcgi?book=gene&part=xp.
- ERCC5 wikiPageID "14754203".
- ERCC5 wikiPageRevisionID "606489679".
- ERCC5 hasPhotoCollection ERCC5.
- ERCC5 label "arthrogryposis".
- ERCC5 requireManualInspection "no".
- ERCC5 summaryText "Excision repair cross-complementing rodent repair deficiency, complementation group 5 is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Multiple alternatively spliced transcript variants encoding distinct isoforms have been described, but the biological validity of all variants has not been determined.".
- ERCC5 target "arthrogryposis".
- ERCC5 type "mutation_results_in".
- ERCC5 updateCitations "yes".
- ERCC5 updatePage "yes".
- ERCC5 updateProteinBox "yes".
- ERCC5 updateSummary "yes".
- ERCC5 type Biomolecule.
- ERCC5 type Protein.
- ERCC5 type BiologicalObject.
- ERCC5 comment "DNA repair protein complementing XP-G cells is a protein that in humans is encoded by the ERCC5 gene.Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia.".
- ERCC5 label "ERCC5".
- ERCC5 sameAs m.03gwqj2.
- ERCC5 sameAs Q5324024.
- ERCC5 sameAs Q5324024.
- ERCC5 sameAs ERCC5.
- ERCC5 wasDerivedFrom ERCC5?oldid=606489679.
- ERCC5 isPrimaryTopicOf ERCC5.