abnormal muscle physiology_Egln2<tm1Pec>/Egln2<tm1Pec>

http://metadb.riken.jp/0002106I129SSvEvSwissEgln2tm1PecEgln2tm1PecEgln2tm1Pec

abnormal muscle physiology_Egln2<tm1Pec>/Egln2<tm1Pec>

表現型アノテーション

MGI marker

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

• egl-9 family hypoxia-inducible factor 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1932287

遺伝子型

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

• Egln2<tm1Pec>/Egln2<tm1Pec>

アレルシンボル

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

• Egln2<tm1Pec>

遺伝的背景

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

• involves: 129S/SvEv * Swiss

MP annotation

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

• abnormal muscle physiology
  http://purl.obolibrary.org/obo/MP_0002106

文献

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

• Julián. Aragonés, et.al., Deficiency or inhibition of oxygen sensor Phd1 induces hypoxia tolerance by reprogramming basal metabolism., Nature genetics, 2008, 40
  http://rdf.ncbi.nlm.nih.gov/pubmed/18176562