cochlear ganglion degeneration_Loxhd1<sba>/Loxhd1<sba>

http://metadb.riken.jp/0002857IC57BL6JLoxhd1sbaLoxhd1sbaLoxhd1sba

cochlear ganglion degeneration_Loxhd1<sba>/Loxhd1<sba>

表現型アノテーション

MGI marker

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

• lipoxygenase homology domains 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1914609

遺伝子型

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

• Loxhd1<sba>/Loxhd1<sba>

アレルシンボル

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

• Loxhd1<sba>

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

• cochlear ganglion degeneration
  http://purl.obolibrary.org/obo/MP_0002857

文献

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

• Nicolas. Grillet, et.al., Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans., American journal of human genetics, 2009, 85
  http://rdf.ncbi.nlm.nih.gov/pubmed/19732867