decreased startle reflex_Dfnb59<sti>/Dfnb59<sti>

http://metadb.riken.jp/0001489IC57BL6JDfnb59stiDfnb59stiDfnb59sti

decreased startle reflex_Dfnb59<sti>/Dfnb59<sti>

表現型アノテーション

MGI marker

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

• deafness, autosomal recessive 59 (human)
  http://metadb.riken.jp/db/mgi_rdf/MGI:2685847

遺伝子型

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

• Dfnb59<sti>/Dfnb59<sti>

アレルシンボル

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

• Dfnb59<sti>

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

• decreased startle reflex
  http://purl.obolibrary.org/obo/MP_0001489

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