abnormal sternum ossification_Foxc1<tm1Blh>/Foxc1<tm1Blh>

http://metadb.riken.jp/0008277I129S6SvEvTacBlackSwissFoxc1tm1BlhFoxc1tm1BlhFoxc1tm1Blh

abnormal sternum ossification_Foxc1<tm1Blh>/Foxc1<tm1Blh>

表現型アノテーション

MGI marker

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

• forkhead box C1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1347466

遺伝子型

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

• Foxc1<tm1Blh>/Foxc1<tm1Blh>

アレルシンボル

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

• Foxc1<tm1Blh>

遺伝的背景

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

• involves: 129S6/SvEvTac * Black Swiss

MP annotation

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

• abnormal sternum ossification
  http://purl.obolibrary.org/obo/MP_0008277

文献

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

• T. Kume, et.al., The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus., Cell, 1998, 93
  http://rdf.ncbi.nlm.nih.gov/pubmed/9635428