no abnormal phenotype detected_Apba2<tm1.1Sud>/Apba2<tm1.1Sud>

http://metadb.riken.jp/0002169I129S1Sv129X1SvJApba2tm11SudApba2tm11SudApba2tm11Sud

no abnormal phenotype detected_Apba2<tm1.1Sud>/Apba2<tm1.1Sud>

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-binding, family A, member 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1261791

遺伝子型

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

• Apba2<tm1.1Sud>/Apba2<tm1.1Sud>

アレルシンボル

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

• Apba2<tm1.1Sud>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ

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

• Angela. Ho, et.al., Genetic analysis of Mint/X11 proteins: essential presynaptic functions of a neuronal adaptor protein family., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2006, 26
  http://rdf.ncbi.nlm.nih.gov/pubmed/17167098