Yoshibumi. Matsushima, et.al., A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene., Mammalian genome : official journal of the International Mammalian Genome Society, 2002, 13

http://rdf.ncbi.nlm.nih.gov/pubmed/11773966

Yoshibumi. Matsushima, et.al., A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene., Mammalian genome : official journal of the International Mammalian Genome Society, 2002, 13

pubmed

allele

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

• Ednrb<WS4>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2674291

表現型アノテーション

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

• deafness_Ednrb<WS4>/Ednrb<WS4>
  http://metadb.riken.jp/0001967IBALBcMSMEdnrbWS4EdnrbWS4EdnrbWS4
• abnormal cochlea morphology_Ednrb<WS4>/Ednrb<WS4>
  http://metadb.riken.jp/0000031IBALBcMSMEdnrbWS4EdnrbWS4EdnrbWS4
• abnormal hearing physiology_Ednrb<WS4>/Ednrb<WS4>
  http://metadb.riken.jp/0001963IBALBcMSMEdnrbWS4EdnrbWS4EdnrbWS4
• thin stria vascularis_Ednrb<WS4>/Ednrb<WS4>
  http://metadb.riken.jp/0004364IBALBcMSMEdnrbWS4EdnrbWS4EdnrbWS4
• megacolon_Ednrb<WS4>/Ednrb<WS4>
  http://metadb.riken.jp/0002731IBALBcMSMEdnrbWS4EdnrbWS4EdnrbWS4
• absent strial intermediate cells_Ednrb<WS4>/Ednrb<WS4>
  http://metadb.riken.jp/0006010IBALBcMSMEdnrbWS4EdnrbWS4EdnrbWS4
• cochlear hair cell degeneration_Ednrb<WS4>/Ednrb<WS4>
  http://metadb.riken.jp/0004362IBALBcMSMEdnrbWS4EdnrbWS4EdnrbWS4
• organ of Corti degeneration_Ednrb<WS4>/Ednrb<WS4>
  http://metadb.riken.jp/0000043IBALBcMSMEdnrbWS4EdnrbWS4EdnrbWS4
• abnormal stria vascularis morphology_Ednrb<WS4>/Ednrb<WS4>
  http://metadb.riken.jp/0000048IBALBcMSMEdnrbWS4EdnrbWS4EdnrbWS4
• variable body spotting_Ednrb<WS4>/Ednrb<WS4>
  http://metadb.riken.jp/0002940IBALBcMSMEdnrbWS4EdnrbWS4EdnrbWS4
• premature death_Ednrb<WS4>/Ednrb<WS4>
  http://metadb.riken.jp/0002083IBALBcMSMEdnrbWS4EdnrbWS4EdnrbWS4

class

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

• Ednrb<WS4>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2674291

article

http://www.w3.org/2000/01/rdf-schema#seeAlso

• [Blank]

BRC マウスの系統

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

• MSM.C-Ednrb<WS4>/StmRbrc
  http://metadb.riken.jp/db/rikenbrc_mouse/RBRC00763

表現型アノテーション

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

• abnormal hearing physiology in RBRC00763
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1001271
• abnormal cochlea morphology in RBRC00763
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1001268
• organ of Corti degeneration in RBRC00763
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1001269
• variable body spotting in RBRC00763
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1001275
• deafness in RBRC00763
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1001272
• megacolon in RBRC00763
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1001274
• abnormal stria vascularis morphology in RBRC00763
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1001270
• premature death in RBRC00763
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1001273
• cochlear hair cell degeneration in RBRC00763
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1001276
• absent strial intermediate cells in RBRC00763
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1001278
• thin stria vascularis in RBRC00763
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1001277

article

http://www.w3.org/2000/01/rdf-schema#seeAlso

• [Blank]