type II spiral ligament fibrocyte degeneration_Slc26a4<tm1Egr>/Slc26a4<tm1Egr>

http://metadb.riken.jp/0004488I129S6SvEvTacSlc26a4tm1EgrSlc26a4tm1EgrSlc26a4tm1Egr

type II spiral ligament fibrocyte degeneration_Slc26a4<tm1Egr>/Slc26a4<tm1Egr>

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 4
  http://metadb.riken.jp/db/mgi_rdf/MGI:1346029

遺伝子型

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

• Slc26a4<tm1Egr>/Slc26a4<tm1Egr>

アレルシンボル

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

• Slc26a4<tm1Egr>

遺伝的背景

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

• involves: 129S6/SvEvTac

MP annotation

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

• type II spiral ligament fibrocyte degeneration
  http://purl.obolibrary.org/obo/MP_0004488

文献

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

• Philine. Wangemann, et.al., Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model., BMC medicine, 2004, 2
  http://rdf.ncbi.nlm.nih.gov/pubmed/15320950