no abnormal phenotype detected_Sox12<tm2.1Weg>/Sox12<tm2.1Weg>

http://metadb.riken.jp/0002169I129C57BL6Sox12tm21WegSox12tm21WegSox12tm21Weg

no abnormal phenotype detected_Sox12<tm2.1Weg>/Sox12<tm2.1Weg>

表現型アノテーション

MGI marker

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

• SRY (sex determining region Y)-box 12
  http://metadb.riken.jp/db/mgi_rdf/MGI:98360

遺伝子型

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

• Sox12<tm2.1Weg>/Sox12<tm2.1Weg>

アレルシンボル

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

• Sox12<tm2.1Weg>

遺伝的背景

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

• involves: 129 * C57BL/6

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

• Pallavi. Bhattaram, et.al., Organogenesis relies on SoxC transcription factors for the survival of neural and mesenchymal progenitors., Nature communications, 2010, 1
  http://rdf.ncbi.nlm.nih.gov/pubmed/20596238