abnormal craniofacial development_Setd2<tm1Zhch>/Setd2<tm1Zhch>

http://metadb.riken.jp/0003935I129S1SvC57BL6Setd2tm1ZhchSetd2tm1ZhchSetd2tm1Zhch

abnormal craniofacial development_Setd2<tm1Zhch>/Setd2<tm1Zhch>

表現型アノテーション

MGI marker

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

• SET domain containing 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1918177

遺伝子型

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

• Setd2<tm1Zhch>/Setd2<tm1Zhch>

アレルシンボル

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

• Setd2<tm1Zhch>

遺伝的背景

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

• involves: 129S1/Sv * C57BL/6

MP annotation

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

• abnormal craniofacial development
  http://purl.obolibrary.org/obo/MP_0003935

文献

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

• Ming. Hu, et.al., Histone H3 lysine 36 methyltransferase Hypb/Setd2 is required for embryonic vascular remodeling., Proceedings of the National Academy of Sciences of the United States of America, 2010, 107
  http://rdf.ncbi.nlm.nih.gov/pubmed/20133625