abnormal cochlea morphology_Foxi1<tm1Sven>/Foxi1<tm1Sven>

http://metadb.riken.jp/0000031ICD1Foxi1tm1SvenFoxi1tm1SvenFoxi1tm1Sven

abnormal cochlea morphology_Foxi1<tm1Sven>/Foxi1<tm1Sven>

表現型アノテーション

MGI marker

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

• forkhead box I1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1096329

遺伝子型

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

• Foxi1<tm1Sven>/Foxi1<tm1Sven>

アレルシンボル

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

• Foxi1<tm1Sven>

遺伝的背景

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

• involves: CD-1

MP annotation

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

• abnormal cochlea morphology
  http://purl.obolibrary.org/obo/MP_0000031

文献

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

• Malin. Hulander, et.al., Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice., Development (Cambridge, England), 2003, 130
  http://rdf.ncbi.nlm.nih.gov/pubmed/12642503