no abnormal phenotype detected_Zfhx3<tm1.1Jtd>/Zfhx3<tm1.1Jtd>

http://metadb.riken.jp/0002169I129S6SvEvTacC57BL6C57BL6JSJLZfhx3tm11JtdZfhx3tm11JtdZfhx3tm11Jtd

no abnormal phenotype detected_Zfhx3<tm1.1Jtd>/Zfhx3<tm1.1Jtd>

表現型アノテーション

MGI marker

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

• zinc finger homeobox 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:99948

遺伝子型

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

• Zfhx3<tm1.1Jtd>/Zfhx3<tm1.1Jtd>

アレルシンボル

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

• Zfhx3<tm1.1Jtd>

遺伝的背景

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

• involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Xiaodong. Sun, et.al., Heterozygous deletion of Atbf1 by the Cre-loxP system in mice causes preweaning mortality., Genesis (New York, N.Y. : 2000), 2012, 50
  http://rdf.ncbi.nlm.nih.gov/pubmed/22644989