abnormal nursing_Foxb1<tm1Pgr>/Foxb1<tm1Pgr>

http://metadb.riken.jp/0001382I129S1Sv129X1SvJC57BL6Foxb1tm1PgrFoxb1tm1PgrFoxb1tm1Pgr

abnormal nursing_Foxb1<tm1Pgr>/Foxb1<tm1Pgr>

表現型アノテーション

MGI marker

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

• forkhead box B1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1927549

遺伝子型

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

• Foxb1<tm1Pgr>/Foxb1<tm1Pgr>

アレルシンボル

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

• Foxb1<tm1Pgr>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * C57BL/6

MP annotation

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

• abnormal nursing
  http://purl.obolibrary.org/obo/MP_0001382

文献

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

• R. Wehr, et.al., Fkh5-deficient mice show dysgenesis in the caudal midbrain and hypothalamic mammillary body., Development (Cambridge, England), 1997, 124
  http://rdf.ncbi.nlm.nih.gov/pubmed/9409663