abnormal craniofacial development_Grhl3<tm1Bogi>/Grhl3<+>

http://metadb.riken.jp/0003935IC57BL6C57BL6JGrhl3tm1BogiGrhl3Grhl3tm1BogiGrhl3

abnormal craniofacial development_Grhl3<tm1Bogi>/Grhl3<+>

表現型アノテーション

MGI marker

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

• grainyhead-like 3 (Drosophila)
  http://metadb.riken.jp/db/mgi_rdf/MGI:2655333

遺伝子型

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

• Grhl3<tm1Bogi>/Grhl3<+>

アレルシンボル

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

• Grhl3<tm1Bogi>|Grhl3<+>

遺伝的背景

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

• involves: C57BL/6 * C57BL/6J

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