no abnormal phenotype detected_Sntb2<tm1Maad>/Sntb2<tm1Maad>

http://metadb.riken.jp/0002169I129P2OlaHsdC57BL6Sntb2tm1MaadSntb2tm1MaadSntb2tm1Maad

no abnormal phenotype detected_Sntb2<tm1Maad>/Sntb2<tm1Maad>

表現型アノテーション

MGI marker

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

• syntrophin, basic 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:101771

遺伝子型

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

• Sntb2<tm1Maad>/Sntb2<tm1Maad>

アレルシンボル

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

• Sntb2<tm1Maad>

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

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

文献

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

• Marvin E. Adams, et.al., Structural abnormalities at neuromuscular synapses lacking multiple syntrophin isoforms., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004, 24
  http://rdf.ncbi.nlm.nih.gov/pubmed/15548643