no abnormal phenotype detected_Eomes<tm1.1Rob>/Eomes<+>,Wnt3<tm1Brd>/Wnt3<+>

http://metadb.riken.jp/0002169I129SSvEv129S7SvEvBrdC57BL6CBAEomestm11RobEomesWnt3tm1BrdWnt3EomesWnt3Wnt3tm1BrdEomestm11Rob

no abnormal phenotype detected_Eomes<tm1.1Rob>/Eomes<+>,Wnt3<tm1Brd>/Wnt3<+>

表現型アノテーション

MGI marker

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

• eomesodermin
  http://metadb.riken.jp/db/mgi_rdf/MGI:1201683
• wingless-type MMTV integration site family, member 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:98955

遺伝子型

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

• Eomes<tm1.1Rob>/Eomes<+>,Wnt3<tm1Brd>/Wnt3<+>

アレルシンボル

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

• Eomes<+>|Wnt3<+>|Wnt3<tm1Brd>|Eomes<tm1.1Rob>

遺伝的背景

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

• involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * CBA

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

• Sebastian J. Arnold, et.al., Pivotal roles for eomesodermin during axis formation, epithelium-to-mesenchyme transition and endoderm specification in the mouse., Development (Cambridge, England), 2008, 135
  http://rdf.ncbi.nlm.nih.gov/pubmed/18171685