L. De Moerlooze, et.al., An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis., Development (Cambridge, England), 2000, 127

http://rdf.ncbi.nlm.nih.gov/pubmed/10631169

L. De Moerlooze, et.al., An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis., Development (Cambridge, England), 2000, 127

pubmed

allele

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

• Fgfr2<tm1Dsn>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2153810
• Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2153811

表現型アノテーション

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

• abnormal pelvic girdle bone morphology_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0004509I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal endolymphatic duct morphology_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0006011I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• absent Rathke's pouch_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0011759I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal ilium morphology_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0005354I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• arrest of tooth development_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0000118I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal limb development_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0006279I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• small stomach_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0002691I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• caudal vertebral fusion_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0004619I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal Rathke's pouch development_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0013351I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• absent forelimb_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0000551I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• thin skin_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0001199I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal lung development_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0001176I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• premature suture closure_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0000081I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal stomach morphology_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0000470I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• small scapula_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0004343I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal ischium morphology_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0004507I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• absent lungs_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0001181I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• absent acromion_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0004346I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• decreased body size_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0001265I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• thin dermal layer_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0001244I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• inner ear cysts_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0006287I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal epidermis stratum basale morphology_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0001231I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• domed cranium_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0000440I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal skin pigmentation_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0002095I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• perinatal lethality, complete penetrance_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0011089I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• absent hypodermis muscle layer_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0011158I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• thin epidermis_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0001218I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal Rathke's pouch apoptosis_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0013352I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal salivary gland morphology_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0000613I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal clavicle morphology_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0005298I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• absent pubis_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0004691I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• curly tail_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0003051I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• absent adenohypophysis_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0008320I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• absent eyelids_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0001341I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• small otic capsule_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0006288I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal pituitary gland development_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0003816I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• abnormal semicircular canal morphology_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0002428I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• translucent skin_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0001201I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• cleft palate_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0000111I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• absent hindlimb_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0000557I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn
• impaired branching involved in trachea morphogenesis_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/0011026I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn

class

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

• Fgfr2<tm1Dsn>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2153810
• Fgfr2<tm1.1Dsn>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2153811