abnormal amino acid level_Gpt2<tm1a(KOMP)Wtsi>/Gpt2<tm1a(KOMP)Wtsi>

http://metadb.riken.jp/0005332IC57BL6JC57BL6NGpt2tm1aKOMPWtsiGpt2tm1aKOMPWtsiGpt2tm1aKOMPWtsi

abnormal amino acid level_Gpt2<tm1a(KOMP)Wtsi>/Gpt2<tm1a(KOMP)Wtsi>

表現型アノテーション

MGI marker

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

• glutamic pyruvate transaminase (alanine aminotransferase) 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1915391

遺伝子型

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

• Gpt2<tm1a(KOMP)Wtsi>/Gpt2<tm1a(KOMP)Wtsi>

アレルシンボル

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

• Gpt2<tm1a(KOMP)Wtsi>

遺伝的背景

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

• involves: C57BL/6J * C57BL/6N

MP annotation

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

• abnormal amino acid level
  http://purl.obolibrary.org/obo/MP_0005332

文献

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

• Qing. Ouyang, et.al., Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features., Proceedings of the National Academy of Sciences of the United States of America, 2016, 113
  http://rdf.ncbi.nlm.nih.gov/pubmed/27601654