no abnormal phenotype detected_Msx2<tm1Yvla>/Msx2<tm1Yvla>

http://metadb.riken.jp/0002169I129S2SvPasC57BL6SJLMsx2tm1YvlaMsx2tm1YvlaMsx2tm1Yvla

no abnormal phenotype detected_Msx2<tm1Yvla>/Msx2<tm1Yvla>

表現型アノテーション

MGI marker

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

• msh homeobox 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:97169

遺伝子型

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

• Msx2<tm1Yvla>/Msx2<tm1Yvla>

アレルシンボル

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

• Msx2<tm1Yvla>

遺伝的背景

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

• involves: 129S2/SvPas * C57BL/6 * 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

• Vardina. Bensoussan, et.al., Generation of an Msx2-GFP conditional null allele., Genesis (New York, N.Y. : 2000), 2008, 46
  http://rdf.ncbi.nlm.nih.gov/pubmed/18442049