axon degeneration_Opa3<m1Votr>/Opa3<m1Votr>

http://metadb.riken.jp/0005405IC3HC57BL6JCrlOpa3m1VotrOpa3m1VotrOpa3m1Votr

axon degeneration_Opa3<m1Votr>/Opa3<m1Votr>

表現型アノテーション

MGI marker

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

• optic atrophy 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:2686271

遺伝子型

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

• Opa3<m1Votr>/Opa3<m1Votr>

アレルシンボル

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

• Opa3<m1Votr>

遺伝的背景

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

• involves: C3H * C57BL/6JCrl

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

• Vanessa J. Davies, et.al., A missense mutation in the murine Opa3 gene models human Costeff syndrome., Brain : a journal of neurology, 2008, 131
  http://rdf.ncbi.nlm.nih.gov/pubmed/18222992