abnormal locomotor activation_App<tm1Cwe>/App<tm1Cwe>

http://metadb.riken.jp/0003313I129S2SvPasApptm1CweApptm1CweApptm1Cwe

abnormal locomotor activation_App<tm1Cwe>/App<tm1Cwe>

表現型アノテーション

MGI marker

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

• amyloid beta (A4) precursor protein
  http://metadb.riken.jp/db/mgi_rdf/MGI:88059

遺伝子型

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

• App<tm1Cwe>/App<tm1Cwe>

アレルシンボル

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

• App<tm1Cwe>

遺伝的背景

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

• involves: 129S2/SvPas

MP annotation

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

• abnormal locomotor activation
  http://purl.obolibrary.org/obo/MP_0003313

文献

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

• Sabine. Ring, et.al., The secreted beta-amyloid precursor protein ectodomain APPs alpha is sufficient to rescue the anatomical, behavioral, and electrophysiological abnormalities of APP-deficient mice., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007, 27
  http://rdf.ncbi.nlm.nih.gov/pubmed/17634375