akinesia_Pgam5<tm1a(EUCOMM)Wtsi>/Pgam5<tm1a(EUCOMM)Wtsi>

http://metadb.riken.jp/0002690IC57BL6NPgam5tm1aEUCOMMWtsiPgam5tm1aEUCOMMWtsiPgam5tm1aEUCOMMWtsi

akinesia_Pgam5<tm1a(EUCOMM)Wtsi>/Pgam5<tm1a(EUCOMM)Wtsi>

表現型アノテーション

MGI marker

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

• phosphoglycerate mutase family member 5
  http://metadb.riken.jp/db/mgi_rdf/MGI:1919792

遺伝子型

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

• Pgam5<tm1a(EUCOMM)Wtsi>/Pgam5<tm1a(EUCOMM)Wtsi>

アレルシンボル

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

• Pgam5<tm1a(EUCOMM)Wtsi>

遺伝的背景

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

• involves: C57BL/6N

MP annotation

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

• akinesia
  http://purl.obolibrary.org/obo/MP_0002690

文献

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

• Wei. Lu, et.al., Genetic deficiency of the mitochondrial protein PGAM5 causes a Parkinson's-like movement disorder., Nature communications, 2014, 5
  http://rdf.ncbi.nlm.nih.gov/pubmed/25222142