delayed inner ear development_Duox2<thyd>/Duox2<thyd>

http://metadb.riken.jp/0004664B6129Duox2thydJDuox2thydDuox2thydDuox2thyd

delayed inner ear development_Duox2<thyd>/Duox2<thyd>

表現型アノテーション

MGI marker

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

• dual oxidase 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:3036280

遺伝子型

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

• Duox2<thyd>/Duox2<thyd>

アレルシンボル

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

• Duox2<thyd>

遺伝的背景

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

• B6(129)-Duox2<thyd>/J

MP annotation

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

• delayed inner ear development
  http://purl.obolibrary.org/obo/MP_0004664

文献

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

• Kenneth R. Johnson, et.al., Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2., Molecular endocrinology (Baltimore, Md.), 2007, 21
  http://rdf.ncbi.nlm.nih.gov/pubmed/17440044