abnormal craniofacial development_Irf6<Gt(OST398253)Lex>/Irf6<+>

http://metadb.riken.jp/0003935I129S5SvEvBrdC57BL6Irf6GtOST398253LexIrf6Irf6GtOST398253LexIrf6

abnormal craniofacial development_Irf6<Gt(OST398253)Lex>/Irf6<+>

表現型アノテーション

MGI marker

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

• interferon regulatory factor 6
  http://metadb.riken.jp/db/mgi_rdf/MGI:1859211

遺伝子型

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

• Irf6<Gt(OST398253)Lex>/Irf6<+>

アレルシンボル

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

• Irf6<Gt(OST398253)Lex>|Irf6<+>

遺伝的背景

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

• involves: 129S5/SvEvBrd * 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

• Myriam. Peyrard-Janvid, et.al., Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development., American journal of human genetics, 2014, 94
  http://rdf.ncbi.nlm.nih.gov/pubmed/24360809