abnormal motor capabilities/coordination/movement_Mecp2<tm6.1Bird>/Y

http://metadb.riken.jp/0002066I129P2OlaHsdC57BL6Mecp2tm61BirdYMecp2tm61Bird

abnormal motor capabilities/coordination/movement_Mecp2<tm6.1Bird>/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 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<tm6.1Bird>/Y

アレルシンボル

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

• Mecp2<tm6.1Bird>

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

• Kyla. Brown, et.al., The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome., Human molecular genetics, 2016, 25
  http://rdf.ncbi.nlm.nih.gov/pubmed/26647311