abnormal behavior_Mecp2<tm1.1Jae>/Y

http://metadb.riken.jp/0004924I129S4SvJaeBALBcC57BL6Mecp2tm11JaeYMecp2tm11Jae

abnormal behavior_Mecp2<tm1.1Jae>/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<tm1.1Jae>/Y

アレルシンボル

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

• Mecp2<tm1.1Jae>

遺伝的背景

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

• involves: 129S4/SvJae * BALB/c * C57BL/6

MP annotation

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

• abnormal behavior
  http://purl.obolibrary.org/obo/MP_0004924

文献

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

• R Z. Chen, et.al., Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice., Nature genetics, 2001, 27
  http://rdf.ncbi.nlm.nih.gov/pubmed/11242118