Y X. Zhou, et.al., A Pro250Arg substitution in mouse Fgfr1 causes increased expression of Cbfa1 and premature fusion of calvarial sutures., Human molecular genetics, 2000, 9

http://rdf.ncbi.nlm.nih.gov/pubmed/10942429

Y X. Zhou, et.al., A Pro250Arg substitution in mouse Fgfr1 causes increased expression of Cbfa1 and premature fusion of calvarial sutures., Human molecular genetics, 2000, 9

pubmed

allele

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

• Fgfr1<tm2Cxd>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2153354
• Fgfr1<tm2.1Cxd>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2153355

class

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

• Fgfr1<tm2Cxd>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2153354
• Fgfr1<tm2.1Cxd>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2153355

表現型アノテーション

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

• premature suture closure_Fgfr1<tm2.1Cxd>/Fgfr1<+>
  http://metadb.riken.jp/0000081I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1Fgfr1Fgfr1tm21Cxd
• midface hypoplasia_Fgfr1<tm2.1Cxd>/Fgfr1<+>
  http://metadb.riken.jp/0012085I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1Fgfr1Fgfr1tm21Cxd
• premature suture closure_Fgfr1<tm2.1Cxd>/Fgfr1<tm2.1Cxd>
  http://metadb.riken.jp/0000081I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1tm21CxdFgfr1tm21Cxd
• increased osteoblast cell number_Fgfr1<tm2.1Cxd>/Fgfr1<+>
  http://metadb.riken.jp/0004988I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1Fgfr1Fgfr1tm21Cxd
• craniofacial asymmetry_Fgfr1<tm2.1Cxd>/Fgfr1<tm2.1Cxd>
  http://metadb.riken.jp/0008863I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1tm21CxdFgfr1tm21Cxd
• ocular hypertelorism_Fgfr1<tm2.1Cxd>/Fgfr1<+>
  http://metadb.riken.jp/0001300I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1Fgfr1Fgfr1tm21Cxd
• decreased body size_Fgfr1<tm2.1Cxd>/Fgfr1<tm2.1Cxd>
  http://metadb.riken.jp/0001265I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1tm21CxdFgfr1tm21Cxd
• abnormal osteoblast physiology_Fgfr1<tm2.1Cxd>/Fgfr1<+>
  http://metadb.riken.jp/0005006I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1Fgfr1Fgfr1tm21Cxd
• abnormal craniofacial bone morphology_Fgfr1<tm2.1Cxd>/Fgfr1<+>
  http://metadb.riken.jp/0002116I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1Fgfr1Fgfr1tm21Cxd
• long incisors_Fgfr1<tm2.1Cxd>/Fgfr1<+>
  http://metadb.riken.jp/0004831I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1Fgfr1Fgfr1tm21Cxd
• abnormal craniofacial bone morphology_Fgfr1<tm2.1Cxd>/Fgfr1<tm2.1Cxd>
  http://metadb.riken.jp/0002116I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1tm21CxdFgfr1tm21Cxd
• craniofacial asymmetry_Fgfr1<tm2.1Cxd>/Fgfr1<+>
  http://metadb.riken.jp/0008863I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1Fgfr1Fgfr1tm21Cxd
• ocular hypertelorism_Fgfr1<tm2.1Cxd>/Fgfr1<tm2.1Cxd>
  http://metadb.riken.jp/0001300I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1tm21CxdFgfr1tm21Cxd
• short tail_Fgfr1<tm2.1Cxd>/Fgfr1<tm2.1Cxd>
  http://metadb.riken.jp/0000592I129S6SvEvTacFVBNFgfr1tm21CxdFgfr1tm21CxdFgfr1tm21Cxd