abnormal skin pigmentation_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>

http://metadb.riken.jp/0002095I129P2OlaHsdC57BL6Fgfr2tm11DsnFgfr2tm11DsnFgfr2tm11Dsn

abnormal skin pigmentation_Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>

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 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:95523

遺伝子型

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

• Fgfr2<tm1.1Dsn>/Fgfr2<tm1.1Dsn>

アレルシンボル

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

• Fgfr2<tm1.1Dsn>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6

MP annotation

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

• abnormal skin pigmentation
  http://purl.obolibrary.org/obo/MP_0002095

文献

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

• 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