no abnormal phenotype detected_Sox2<tm1.1Vep>/Sox2<+>

http://metadb.riken.jp/0002169NSSox2tm11VepSox2Sox2Sox2tm11Vep

no abnormal phenotype detected_Sox2<tm1.1Vep>/Sox2<+>

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 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:98364

遺伝子型

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

• Sox2<tm1.1Vep>/Sox2<+>

アレルシンボル

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

• Sox2<+>|Sox2<tm1.1Vep>

遺伝的背景

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

• Not Specified

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

• Antigoni. Ekonomou, et.al., Neuronal migration and ventral subtype identity in the telencephalon depend on SOX1., PLoS biology, 2005, 3
  http://rdf.ncbi.nlm.nih.gov/pubmed/15882093