cochlear hair cell degeneration_Ednrb<WS4>/Ednrb<WS4>

http://metadb.riken.jp/0004362IBALBcMSMEdnrbWS4EdnrbWS4EdnrbWS4

cochlear hair cell degeneration_Ednrb<WS4>/Ednrb<WS4>

表現型アノテーション

MGI marker

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

• endothelin receptor type B
  http://metadb.riken.jp/db/mgi_rdf/MGI:102720

遺伝子型

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

• Ednrb<WS4>/Ednrb<WS4>

アレルシンボル

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

• Ednrb<WS4>

遺伝的背景

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

• involves: BALB/c * MSM

MP annotation

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

• cochlear hair cell degeneration
  http://purl.obolibrary.org/obo/MP_0004362

文献

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

• 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