myopathy_Stmn1<tm1Wed>/Stmn1<tm1Wed>

http://metadb.riken.jp/0000751I129P2OlaHsdC57BL6Stmn1tm1WedStmn1tm1WedStmn1tm1Wed

myopathy_Stmn1<tm1Wed>/Stmn1<tm1Wed>

表現型アノテーション

MGI marker

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

• stathmin 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:96739

遺伝子型

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

• Stmn1<tm1Wed>/Stmn1<tm1Wed>

アレルシンボル

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

• Stmn1<tm1Wed>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6

MP annotation

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

• myopathy
  http://purl.obolibrary.org/obo/MP_0000751

文献

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

• Wolfgang. Liedtke, et.al., Stathmin-deficient mice develop an age-dependent axonopathy of the central and peripheral nervous systems., The American journal of pathology, 2002, 160
  http://rdf.ncbi.nlm.nih.gov/pubmed/11839567