abnormal locomotor behavior_Mecp2<tm1Hzo>/Y

http://metadb.riken.jp/0001392I129S7SvEvBrdC57BL6JMecp2tm1HzoYMecp2tm1Hzo

abnormal locomotor behavior_Mecp2<tm1Hzo>/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 protein 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:99918

遺伝子型

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

• Mecp2<tm1Hzo>/Y

アレルシンボル

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

• Mecp2<tm1Hzo>

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

• abnormal locomotor behavior
  http://purl.obolibrary.org/obo/MP_0001392

文献

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

• Mona. Shahbazian, et.al., Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3., Neuron, 2002, 35
  http://rdf.ncbi.nlm.nih.gov/pubmed/12160743