cochlear hair cell degeneration_Myo6<sv>/Myo6<sv>

http://metadb.riken.jp/0004362IB10HA33NXSnC57BL6JMyo6svMyo6svMyo6sv

cochlear hair cell 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 * C57BL/6J

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

• K B. Avraham, et.al., The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells., Nature genetics, 1995, 11
  http://rdf.ncbi.nlm.nih.gov/pubmed/7493015