abnormal basisphenoid bone morphology_Fgfr1<tm2.1Cxd>/Fgfr1<+>

http://metadb.riken.jp/0000106D2129S6CgFgfr1tm21CxdFgfr1tm21CxdFgfr1Fgfr1tm21CxdFgfr1

abnormal basisphenoid bone morphology_Fgfr1<tm2.1Cxd>/Fgfr1<+>

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 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:95522

遺伝子型

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

• Fgfr1<tm2.1Cxd>/Fgfr1<+>

アレルシンボル

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

• Fgfr1<tm2.1Cxd>|Fgfr1<+>

遺伝的背景

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

• D2.129S6(Cg)-Fgfr1<tm2.1Cxd>

MP annotation

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

• abnormal basisphenoid bone morphology
  http://purl.obolibrary.org/obo/MP_0000106

文献

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

• Roopa. Purushothaman, et.al., Facial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromes., Birth defects research. Part A, Clinical and molecular teratology, 2011, 91
  http://rdf.ncbi.nlm.nih.gov/pubmed/21538817