abnormal craniofacial development_Wdr19<twto>/Wdr19<twto>

http://metadb.riken.jp/0003935IFVBNJWdr19twtoWdr19twtoWdr19twto

abnormal craniofacial development_Wdr19<twto>/Wdr19<twto>

表現型アノテーション

MGI marker

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

• WD repeat domain 19
  http://metadb.riken.jp/db/mgi_rdf/MGI:2443231

遺伝子型

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

• Wdr19<twto>/Wdr19<twto>

アレルシンボル

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

• Wdr19<twto>

遺伝的背景

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

• involves: FVB/NJ

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

• Alyson. Ashe, et.al., Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies., Human molecular genetics, 2012, 21
  http://rdf.ncbi.nlm.nih.gov/pubmed/22228095