impaired swimming_Myo6<twt>/Myo6<twt>

http://metadb.riken.jp/0001522IC57BL6JMyo6twtMyo6twtMyo6twt

impaired swimming_Myo6<twt>/Myo6<twt>

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<twt>/Myo6<twt>

アレルシンボル

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

• Myo6<twt>

遺伝的背景

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

• involves: C57BL/6J

MP annotation

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

• impaired swimming
  http://purl.obolibrary.org/obo/MP_0001522

文献

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

• Martin. Schwander, et.al., A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007, 27
  http://rdf.ncbi.nlm.nih.gov/pubmed/17329413