short mandible_Fgfr2<tm1Ewj>/Fgfr2<+>,Tg(EIIa-cre)C5379Lmgd/0

http://metadb.riken.jp/0000088B6CgFgfr2tm1EwjTgEIIacreC5379LmgdFgfr2tm1EwjFgfr2TgEIIacreC5379Lmgd0Fgfr2TgEIIacreC5379LmgdFgfr2tm1Ewj

short mandible_Fgfr2<tm1Ewj>/Fgfr2<+>,Tg(EIIa-cre)C5379Lmgd/0

表現型アノテーション

MGI marker

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

• transgene insertion C5379, Laboratory of Mammalian Genes and Development, Heiner Westphal
  http://metadb.riken.jp/db/mgi_rdf/MGI:2137685
• 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<tm1Ewj>/Fgfr2<+>,Tg(EIIa-cre)C5379Lmgd/0

アレルシンボル

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

• Fgfr2<+>|Tg(EIIa-cre)C5379Lmgd|Fgfr2<tm1Ewj>

遺伝的背景

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

• B6.Cg-Fgfr2<tm1Ewj> Tg(EIIa-cre)C5379Lmgd

MP annotation

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

• short mandible
  http://purl.obolibrary.org/obo/MP_0000088

文献

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

• Yingli. Wang, et.al., Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) mice., BMC developmental biology, 2010, 10
  http://rdf.ncbi.nlm.nih.gov/pubmed/20175913