no abnormal phenotype detected_Aplp2<tm1.1Umu>/Aplp2<tm1.1Umu>

http://metadb.riken.jp/0002169I129P2OlaHsdC57BL6NAplp2tm11UmuAplp2tm11UmuAplp2tm11Umu

no abnormal phenotype detected_Aplp2<tm1.1Umu>/Aplp2<tm1.1Umu>

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-like protein 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:88047

遺伝子型

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

• Aplp2<tm1.1Umu>/Aplp2<tm1.1Umu>

アレルシンボル

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

• Aplp2<tm1.1Umu>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6N

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Jan-Philipp. Mallm, et.al., Generation of conditional null alleles for APP and APLP2., Genesis (New York, N.Y. : 2000), 2010, 48
  http://rdf.ncbi.nlm.nih.gov/pubmed/20140888