cochlear degeneration_Myo6<sv>/Myo6<sv>

http://metadb.riken.jp/0000032IB10HA33NXSnSEC1GnMyo6svMyo6svMyo6sv

cochlear degeneration_Myo6<sv>/Myo6<sv>

表現型アノテーション

MGI marker

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

• myosin VI
  http://metadb.riken.jp/db/mgi_rdf/MGI:104785

遺伝子型

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

• Myo6<sv>/Myo6<sv>

アレルシンボル

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

• Myo6<sv>

遺伝的背景

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

• involves: B10.HA/(33NX)Sn * SEC/1Gn

MP annotation

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

• cochlear degeneration
  http://purl.obolibrary.org/obo/MP_0000032

文献

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

• M S. Deol, et.al., Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse., Genetical research, 1966, 8
  http://rdf.ncbi.nlm.nih.gov/pubmed/5980120