absent presphenoid bone_Ptch1<dl>/Ptch1<dl>

http://metadb.riken.jp/0004449I129S1SvImJC57BL6JPtch1dlPtch1dlPtch1dl

absent presphenoid bone_Ptch1<dl>/Ptch1<dl>

表現型アノテーション

MGI marker

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

• patched 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:105373

遺伝子型

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

• Ptch1<dl>/Ptch1<dl>

アレルシンボル

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

• Ptch1<dl>

遺伝的背景

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

• involves: 129S1/SvImJ * C57BL/6J

MP annotation

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

• absent presphenoid bone
  http://purl.obolibrary.org/obo/MP_0004449

文献

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

• Weiguo. Feng, et.al., The Ptch1(DL) mouse: a new model to study lambdoid craniosynostosis and basal cell nevus syndrome-associated skeletal defects., Genesis (New York, N.Y. : 2000), 2013, 51
  http://rdf.ncbi.nlm.nih.gov/pubmed/23897749