abnormal mitochondrial ATP synthesis coupled electron transport_Sco2<tm1.1Easc>/Sco2<tm2.1Easc>

http://metadb.riken.jp/0010956129X1SvJSco2tm11EascSco2tm21EascSco2tm11EascSco2tm21EascSco2tm21EascSco2tm11Easc

abnormal mitochondrial ATP synthesis coupled electron transport_Sco2<tm1.1Easc>/Sco2<tm2.1Easc>

表現型アノテーション

MGI marker

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

• SCO2 cytochrome c oxidase assembly protein
  http://metadb.riken.jp/db/mgi_rdf/MGI:3818630

遺伝子型

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

• Sco2<tm1.1Easc>/Sco2<tm2.1Easc>

アレルシンボル

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

• Sco2<tm2.1Easc>|Sco2<tm1.1Easc>

遺伝的背景

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

• 129X1/SvJ-Sco2<tm1.1Easc>/Sco2<tm2.1Easc>

MP annotation

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

• abnormal mitochondrial ATP synthesis coupled electron transport
  http://purl.obolibrary.org/obo/MP_0010956

文献

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

• Hua. Yang, et.al., Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2., Human molecular genetics, 2010, 19
  http://rdf.ncbi.nlm.nih.gov/pubmed/19837698