abnormal cochlear nerve compound action potential_Otoa<tm1Gpr>/Otoa<tm1Gpr>

http://metadb.riken.jp/0004415I129SSvEvOtoatm1GprOtoatm1GprOtoatm1Gpr

abnormal cochlear nerve compound action potential_Otoa<tm1Gpr>/Otoa<tm1Gpr>

表現型アノテーション

MGI marker

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

• otoancorin
  http://metadb.riken.jp/db/mgi_rdf/MGI:2149209

遺伝子型

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

• Otoa<tm1Gpr>/Otoa<tm1Gpr>

アレルシンボル

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

• Otoa<tm1Gpr>

遺伝的背景

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

• involves: 129S/SvEv

MP annotation

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

• abnormal cochlear nerve compound action potential
  http://purl.obolibrary.org/obo/MP_0004415

文献

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

• Andrei N. Lukashkin, et.al., A mouse model for human deafness DFNB22 reveals that hearing impairment is due to a loss of inner hair cell stimulation., Proceedings of the National Academy of Sciences of the United States of America, 2012, 109
  http://rdf.ncbi.nlm.nih.gov/pubmed/23129639