microcephaly_Satb2<tm1(cre)Vit>/Satb2<tm1(cre)Vit>

http://metadb.riken.jp/0000433IC57BL6Satb2tm1creVitSatb2tm1creVitSatb2tm1creVit

microcephaly_Satb2<tm1(cre)Vit>/Satb2<tm1(cre)Vit>

表現型アノテーション

MGI marker

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

• special AT-rich sequence binding protein 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:2679336

遺伝子型

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

• Satb2<tm1(cre)Vit>/Satb2<tm1(cre)Vit>

アレルシンボル

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

• Satb2<tm1(cre)Vit>

遺伝的背景

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

• involves: C57BL/6

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• microcephaly
  http://purl.obolibrary.org/obo/MP_0000433

文献

http://purl.org/net/cito/citesAsAuthority

• Olga. Britanova, et.al., Satb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw development., American journal of human genetics, 2006, 79
  http://rdf.ncbi.nlm.nih.gov/pubmed/16960803