abnormal mitochondrial ATP synthesis coupled electron transport_Pdss2<kd>/Pdss2<kd>

http://metadb.riken.jp/0010956IC57BL6CBAHPdss2kdPdss2kdPdss2kd

abnormal mitochondrial ATP synthesis coupled electron transport_Pdss2<kd>/Pdss2<kd>

表現型アノテーション

MGI marker

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

• prenyl (solanesyl) diphosphate synthase, subunit 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1918615

遺伝子型

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

• Pdss2<kd>/Pdss2<kd>

アレルシンボル

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

• Pdss2<kd>

遺伝的背景

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

• involves: C57BL/6 * CBA/H

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

• Min. Peng, et.al., Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal disease., PLoS genetics, 2008, 4
  http://rdf.ncbi.nlm.nih.gov/pubmed/18437205