decreased cochlear nerve compound action potential_Emx2<Pdo>/Emx2<+>

http://metadb.riken.jp/0004417IBALBcC3HHeNEmx2PdoEmx2Emx2PdoEmx2

decreased cochlear nerve compound action potential_Emx2<Pdo>/Emx2<+>

表現型アノテーション

MGI marker

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

• empty spiracles homeobox 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:95388

遺伝子型

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

• Emx2<Pdo>/Emx2<+>

アレルシンボル

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

• Emx2<Pdo>|Emx2<+>

遺伝的背景

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

• involves: BALB/c * C3H/HeN

MP annotation

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

• decreased cochlear nerve compound action potential
  http://purl.obolibrary.org/obo/MP_0004417

文献

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

• Charlotte R. Rhodes, et.al., The homeobox gene Emx2 underlies middle ear and inner ear defects in the deaf mouse mutant pardon., Journal of neurocytology, 2003, 32
  http://rdf.ncbi.nlm.nih.gov/pubmed/15044845