inner ear hypoplasia_Lmx1a<bsd>/Lmx1a<bsd>

http://metadb.riken.jp/0006286I129S5SvEvBrdLmx1absdLmx1absdLmx1absd

inner ear hypoplasia_Lmx1a<bsd>/Lmx1a<bsd>

表現型アノテーション

MGI marker

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

• LIM homeobox transcription factor 1 alpha
  http://metadb.riken.jp/db/mgi_rdf/MGI:1888519

遺伝子型

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

• Lmx1a<bsd>/Lmx1a<bsd>

アレルシンボル

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

• Lmx1a<bsd>

遺伝的背景

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

• involves: 129S5/SvEvBrd

MP annotation

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

• inner ear hypoplasia
  http://purl.obolibrary.org/obo/MP_0006286

文献

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

• Georg. Steffes, et.al., Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) are two new mutations of Lmx1a causing severe cochlear and vestibular defects., PloS one, 2012, 7
  http://rdf.ncbi.nlm.nih.gov/pubmed/23226461