no abnormal phenotype detected_Med12<tm1.1Hsch>/Y

http://metadb.riken.jp/0002169I129S6SvEvTacC57BL6NCrMed12tm11HschYMed12tm11Hsch

no abnormal phenotype detected_Med12<tm1.1Hsch>/Y

表現型アノテーション

MGI marker

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

• mediator complex subunit 12
  http://metadb.riken.jp/db/mgi_rdf/MGI:1926212

遺伝子型

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

• Med12<tm1.1Hsch>/Y

アレルシンボル

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

• Med12<tm1.1Hsch>

遺伝的背景

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

• involves: 129S6/SvEvTac * C57BL/6NCr

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

• Pedro P. Rocha, et.al., Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling., Development (Cambridge, England), 2010, 137
  http://rdf.ncbi.nlm.nih.gov/pubmed/20630950