absent occipital bone_Tgfb2<tm1Doe>/Tgfb2<tm1Doe>

http://metadb.riken.jp/0004440I129P2OlaHsdBlackSwissTgfb2tm1DoeTgfb2tm1DoeTgfb2tm1Doe

absent occipital bone_Tgfb2<tm1Doe>/Tgfb2<tm1Doe>

表現型アノテーション

MGI marker

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

• transforming growth factor, beta 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:98726

遺伝子型

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

• Tgfb2<tm1Doe>/Tgfb2<tm1Doe>

アレルシンボル

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

• Tgfb2<tm1Doe>

遺伝的背景

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

• involves: 129P2/OlaHsd * Black Swiss

MP annotation

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

• absent occipital bone
  http://purl.obolibrary.org/obo/MP_0004440

文献

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

• L P. Sanford, et.al., TGFbeta2 knockout mice have multiple developmental defects that are non-overlapping with other TGFbeta knockout phenotypes., Development (Cambridge, England), 1997, 124
  http://rdf.ncbi.nlm.nih.gov/pubmed/9217007