abnormal motor capabilities/coordination/movement_Mbd2<tm1Bh>/Mbd2<tm1Bh>,Mecp2<tm1.1Bird>/Y

http://metadb.riken.jp/0002066I129P2OlaHsdC57BL6Mbd2tm1BhMbd2tm1BhMecp2tm11BirdYMecp2tm11BirdMbd2tm1Bh

abnormal motor capabilities/coordination/movement_Mbd2<tm1Bh>/Mbd2<tm1Bh>,Mecp2<tm1.1Bird>/Y

表現型アノテーション

MGI marker

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

• methyl-CpG binding domain protein 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1333813
• methyl CpG binding protein 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:99918

遺伝子型

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

• Mbd2<tm1Bh>/Mbd2<tm1Bh>,Mecp2<tm1.1Bird>/Y

アレルシンボル

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

• Mecp2<tm1.1Bird>|Mbd2<tm1Bh>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6

MP annotation

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

• abnormal motor capabilities/coordination/movement
  http://purl.obolibrary.org/obo/MP_0002066

文献

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

• J. Guy, et.al., A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome., Nature genetics, 2001, 27
  http://rdf.ncbi.nlm.nih.gov/pubmed/11242117