myopathy_Cox10<tm1Ctm>/Cox10<tm1Ctm>,Myl1<tm1(cre)Sjb>/Myl1<+>

http://metadb.riken.jp/0000751I129X1SvJC57BL6Cox10tm1CtmCox10tm1CtmMyl1tm1creSjbMyl1Myl1Myl1tm1creSjbCox10tm1Ctm

myopathy_Cox10<tm1Ctm>/Cox10<tm1Ctm>,Myl1<tm1(cre)Sjb>/Myl1<+>

表現型アノテーション

MGI marker

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

• cytochrome c oxidase assembly protein 10
  http://metadb.riken.jp/db/mgi_rdf/MGI:1917633
• myosin, light polypeptide 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:97269

遺伝子型

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

• Cox10<tm1Ctm>/Cox10<tm1Ctm>,Myl1<tm1(cre)Sjb>/Myl1<+>

アレルシンボル

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

• Myl1<+>|Myl1<tm1(cre)Sjb>|Cox10<tm1Ctm>

遺伝的背景

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

• involves: 129X1/SvJ * 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

• Francisca. Diaz, et.al., Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency., Human molecular genetics, 2005, 14
  http://rdf.ncbi.nlm.nih.gov/pubmed/16103131