absent linear vestibular evoked potential_Kcna10<tm1Lex>/Kcna10<tm1Lex>

http://metadb.riken.jp/0004813I129SSvEvBrdC57BL6Kcna10tm1LexKcna10tm1LexKcna10tm1Lex

absent linear vestibular evoked potential_Kcna10<tm1Lex>/Kcna10<tm1Lex>

表現型アノテーション

MGI marker

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

• potassium voltage-gated channel, shaker-related subfamily, member 10
  http://metadb.riken.jp/db/mgi_rdf/MGI:3037820

遺伝子型

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

• Kcna10<tm1Lex>/Kcna10<tm1Lex>

アレルシンボル

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

• Kcna10<tm1Lex>

遺伝的背景

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

• involves: 129S/SvEvBrd * C57BL/6

MP annotation

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

• absent linear vestibular evoked potential
  http://purl.obolibrary.org/obo/MP_0004813

文献

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

• Sue I. Lee, et.al., A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction., Hearing research, 2013, 300
  http://rdf.ncbi.nlm.nih.gov/pubmed/23528307