impaired hearing_Slc26a5<tm1Jnz>/Slc26a5<+>

http://metadb.riken.jp/0006325I129S7SvEvBrdC57BL6JSlc26a5tm1JnzSlc26a5Slc26a5tm1JnzSlc26a5

impaired hearing_Slc26a5<tm1Jnz>/Slc26a5<+>

表現型アノテーション

MGI marker

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

• solute carrier family 26, member 5
  http://metadb.riken.jp/db/mgi_rdf/MGI:1933154

遺伝子型

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

• Slc26a5<tm1Jnz>/Slc26a5<+>

アレルシンボル

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

• Slc26a5<tm1Jnz>|Slc26a5<+>

遺伝的背景

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

• involves: 129S7/SvEvBrd * C57BL/6J

MP annotation

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

• impaired hearing
  http://purl.obolibrary.org/obo/MP_0006325

文献

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

• M Charles. Liberman, et.al., Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier., Nature, 2002, 419
  http://rdf.ncbi.nlm.nih.gov/pubmed/12239568
• M A. Cheatham, et.al., Cochlear function in mice with only one copy of the prestin gene., The Journal of physiology, 2005, 569
  http://rdf.ncbi.nlm.nih.gov/pubmed/16166160