axon degeneration_Aspa<nur7>/Aspa<nur7>

http://metadb.riken.jp/0005405IC57BL6JAspanur7Aspanur7Aspanur7

axon degeneration_Aspa<nur7>/Aspa<nur7>

表現型アノテーション

MGI marker

http://metadb.riken.jp/db/mgi_rdf/variant_of

• aspartoacylase
  http://metadb.riken.jp/db/mgi_rdf/MGI:87914

遺伝子型

http://metadb.riken.jp/db/mgi_rdf/allele_composition

• Aspa<nur7>/Aspa<nur7>

アレルシンボル

http://metadb.riken.jp/db/mgi_rdf/allele_symbol

• Aspa<nur7>

遺伝的背景

http://metadb.riken.jp/db/mgi_rdf/genetic_background

• involves: C57BL/6J

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• axon degeneration
  http://purl.obolibrary.org/obo/MP_0005405

文献

http://purl.org/net/cito/citesAsAuthority

• Maria. Traka, et.al., Nur7 is a nonsense mutation in the mouse aspartoacylase gene that causes spongy degeneration of the CNS., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2008, 28
  http://rdf.ncbi.nlm.nih.gov/pubmed/18987190
• Helena. Maier, et.al., N-Acetylaspartate Synthase Deficiency Corrects the Myelin Phenotype in a Canavan Disease Mouse Model But Does Not Affect Survival Time., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015, 35
  http://rdf.ncbi.nlm.nih.gov/pubmed/26511242