no abnormal phenotype detected_Fgfr3<tm1Aomw>/Fgfr3<+>

http://metadb.riken.jp/0002169I129P2OlaHsdFgfr3tm1AomwFgfr3Fgfr3Fgfr3tm1Aomw

no abnormal phenotype detected_Fgfr3<tm1Aomw>/Fgfr3<+>

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<tm1Aomw>/Fgfr3<+>

アレルシンボル

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

• Fgfr3<+>|Fgfr3<tm1Aomw>

遺伝的背景

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

• involves: 129P2/OlaHsd

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

• Stephen R F. Twigg, et.al., Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome., Developmental dynamics : an official publication of the American Association of Anatomists, 2009, 238
  http://rdf.ncbi.nlm.nih.gov/pubmed/19086028