lethargy_Oat<tm1Dva>/Oat<tm1Dva>

http://metadb.riken.jp/0005202I129S7SvEvBrdC57BL6JOattm1DvaOattm1DvaOattm1Dva

lethargy_Oat<tm1Dva>/Oat<tm1Dva>

表現型アノテーション

MGI marker

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

• ornithine aminotransferase
  http://metadb.riken.jp/db/mgi_rdf/MGI:97394

遺伝子型

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

• Oat<tm1Dva>/Oat<tm1Dva>

アレルシンボル

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

• Oat<tm1Dva>

遺伝的背景

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

• involves: 129S7/SvEvBrd * C57BL/6J

MP annotation

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

• lethargy
  http://purl.obolibrary.org/obo/MP_0005202

文献

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

• T. Wang, et.al., Mice lacking ornithine-delta-aminotransferase have paradoxical neonatal hypoornithinaemia and retinal degeneration., Nature genetics, 1995, 11
  http://rdf.ncbi.nlm.nih.gov/pubmed/7550347