axon degeneration_Tg(Pmp22)My41Clh/0

http://metadb.riken.jp/0005405IC57BL6JCBACaTgPmp22My41Clh0TgPmp22My41Clh

axon degeneration_Tg(Pmp22)My41Clh/0

表現型アノテーション

MGI marker

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

• transgene insertion My41, Clare Huxley
  http://metadb.riken.jp/db/mgi_rdf/MGI:3794527

遺伝子型

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

• Tg(Pmp22)My41Clh/0

アレルシンボル

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

• Tg(Pmp22)My41Clh

遺伝的背景

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

• involves: C57BL/6J * CBA/Ca

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

• A M. Robertson, et.al., Comparison of a new pmp22 transgenic mouse line with other mouse models and human patients with CMT1A., Journal of anatomy, 2002, 200
  http://rdf.ncbi.nlm.nih.gov/pubmed/12090404