absent presphenoid bone_Fgfr2<m1Sgg>/Fgfr2<m1Sgg>

http://metadb.riken.jp/0004449IC3HHeJC57BL6JFgfr2m1SggFgfr2m1SggFgfr2m1Sgg

absent presphenoid bone_Fgfr2<m1Sgg>/Fgfr2<m1Sgg>

表現型アノテーション

MGI marker

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

• fibroblast growth factor receptor 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:95523

遺伝子型

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

• Fgfr2<m1Sgg>/Fgfr2<m1Sgg>

アレルシンボル

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

• Fgfr2<m1Sgg>

遺伝的背景

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

• involves: C3H/HeJ * C57BL/6J

MP annotation

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

• absent presphenoid bone
  http://purl.obolibrary.org/obo/MP_0004449

文献

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

• S. Mai, et.al., The missense mutation W290R in Fgfr2 causes developmental defects from aberrant IIIb and IIIc signaling., Developmental dynamics : an official publication of the American Association of Anatomists, 2010, 239
  http://rdf.ncbi.nlm.nih.gov/pubmed/20503384