no abnormal phenotype detected_Fgfr3<tm2Cxd>/Fgfr3<tm2Cxd>

http://metadb.riken.jp/0002169I129S6SvEvTacNIHBlackSwissFgfr3tm2CxdFgfr3tm2CxdFgfr3tm2Cxd

no abnormal phenotype detected_Fgfr3<tm2Cxd>/Fgfr3<tm2Cxd>

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 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:95524

遺伝子型

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

• Fgfr3<tm2Cxd>/Fgfr3<tm2Cxd>

アレルシンボル

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

• Fgfr3<tm2Cxd>

遺伝的背景

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

• involves: 129S6/SvEvTac * NIH Black Swiss

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• C. Li, et.al., A Lys644Glu substitution in fibroblast growth factor receptor 3 (FGFR3) causes dwarfism in mice by activation of STATs and ink4 cell cycle inhibitors., Human molecular genetics, 1999, 8
  http://rdf.ncbi.nlm.nih.gov/pubmed/9887329