myopathy_Coq9<tm1.1Lcl>/Coq9<tm1.1Lcl>

http://metadb.riken.jp/0000751IC57BL6C57BL6NTacSJLCoq9tm11LclCoq9tm11LclCoq9tm11Lcl

myopathy_Coq9<tm1.1Lcl>/Coq9<tm1.1Lcl>

表現型アノテーション

MGI marker

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

• coenzyme Q9
  http://metadb.riken.jp/db/mgi_rdf/MGI:1915164

遺伝子型

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

• Coq9<tm1.1Lcl>/Coq9<tm1.1Lcl>

アレルシンボル

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

• Coq9<tm1.1Lcl>

遺伝的背景

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

• involves: C57BL/6 * C57BL/6NTac * SJL

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

• Laura. García-Corzo, et.al., Dysfunctional Coq9 protein causes predominant encephalomyopathy associated with CoQ deficiency., Human molecular genetics, 2013, 22
  http://rdf.ncbi.nlm.nih.gov/pubmed/23255162