abnormal embryo development_Shb<tm1.1Miwe>/Shb<+>

http://metadb.riken.jp/0001672I129X1SvJC57BL6FVBNShbtm11MiweShbShbShbtm11Miwe

abnormal embryo development_Shb<tm1.1Miwe>/Shb<+>

表現型アノテーション

MGI marker

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

• src homology 2 domain-containing transforming protein B
  http://metadb.riken.jp/db/mgi_rdf/MGI:98294

遺伝子型

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

• Shb<tm1.1Miwe>/Shb<+>

アレルシンボル

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

• Shb<+>|Shb<tm1.1Miwe>

遺伝的背景

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

• involves: 129X1/SvJ * C57BL/6 * FVB/N

MP annotation

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

• abnormal embryogenesis/ development
  http://purl.obolibrary.org/obo/MP_0001672

文献

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

• Vitezslav. Kriz, et.al., Shb null allele is inherited with a transmission ratio distortion and causes reduced viability in utero., Developmental dynamics : an official publication of the American Association of Anatomists, 2007, 236
  http://rdf.ncbi.nlm.nih.gov/pubmed/17676633