abnormal frontonasal prominence morphology_knyn/knyn

http://metadb.riken.jp/0009901IC3HHeHC57BL6JAnuknynknynknyn

abnormal frontonasal prominence morphology_knyn/knyn

表現型アノテーション

MGI marker

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

• kanyon
  http://metadb.riken.jp/db/mgi_rdf/MGI:5448845

遺伝子型

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

• knyn/knyn

アレルシンボル

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

• knyn

遺伝的背景

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

• involves: C3H/HeH * C57BL/6JAnu

MP annotation

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

• abnormal frontonasal prominence morphology
  http://purl.obolibrary.org/obo/MP_0009901

文献

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

• Georgina. Caruana, et.al., Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease., PloS one, 2013, 8
  http://rdf.ncbi.nlm.nih.gov/pubmed/23469164