cochlear ganglion degeneration_Slc9a1<swe>/Slc9a1<swe>

http://metadb.riken.jp/0002857B6SJLSlc9a1sweSlc9a1sweSlc9a1sweSlc9a1swe

cochlear ganglion degeneration_Slc9a1<swe>/Slc9a1<swe>

表現型アノテーション

MGI marker

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

• solute carrier family 9 (sodium/hydrogen exchanger), member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:102462

遺伝子型

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

• Slc9a1<swe>/Slc9a1<swe>

アレルシンボル

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

• Slc9a1<swe>

遺伝的背景

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

• B6.SJL-Slc9a1<swe>

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

• G A. Cox, et.al., Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice., Cell, 1997, 91
  http://rdf.ncbi.nlm.nih.gov/pubmed/9335342