incomplete embryo turning_Zeb2<tm1.2Yhi>/Zeb2<tm1.2Yhi>

http://metadb.riken.jp/0001701I129S1Sv129X1SvJCD1Zeb2tm12YhiZeb2tm12YhiZeb2tm12Yhi

incomplete embryo turning_Zeb2<tm1.2Yhi>/Zeb2<tm1.2Yhi>

表現型アノテーション

MGI marker

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

• zinc finger E-box binding homeobox 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1344407

遺伝子型

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

• Zeb2<tm1.2Yhi>/Zeb2<tm1.2Yhi>

アレルシンボル

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

• Zeb2<tm1.2Yhi>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * CD-1

MP annotation

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

• incomplete embryo turning
  http://purl.obolibrary.org/obo/MP_0001701

文献

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

• Tom. Van de Putte, et.al., Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome., American journal of human genetics, 2003, 72
  http://rdf.ncbi.nlm.nih.gov/pubmed/12522767