abnormal gait_Mecp2<tm1Bird>/Y,Pvalb<tm1.1(cre)Aibs>/Pvalb<+>

http://metadb.riken.jp/0001406I129P2OlaHsd129S4SvJaeSor129S6SvEvTacC57BL6JC57BL6NCrlMecp2tm1BirdYPvalbtm11creAibsPvalbPvalbtm11creAibsMecp2tm1BirdPvalb

abnormal gait_Mecp2<tm1Bird>/Y,Pvalb<tm1.1(cre)Aibs>/Pvalb<+>

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
• parvalbumin
  http://metadb.riken.jp/db/mgi_rdf/MGI:97821

遺伝子型

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

• Mecp2<tm1Bird>/Y,Pvalb<tm1.1(cre)Aibs>/Pvalb<+>

アレルシンボル

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

• Pvalb<tm1.1(cre)Aibs>|Mecp2<tm1Bird>|Pvalb<+>

遺伝的背景

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

• involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl

MP annotation

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

• abnormal gait
  http://purl.obolibrary.org/obo/MP_0001406

文献

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

• Aya. Ito-Ishida, et.al., Loss of MeCP2 in Parvalbumin-and Somatostatin-Expressing Neurons in Mice Leads to Distinct Rett Syndrome-like Phenotypes., Neuron, 2015, 88
  http://rdf.ncbi.nlm.nih.gov/pubmed/26590342