no abnormal phenotype detected_Porcn<tm1.1Lcm>/Y

http://metadb.riken.jp/0002169I129S1Sv129X1SvJC57BL6Porcntm11LcmYPorcntm11Lcm

no abnormal phenotype detected_Porcn<tm1.1Lcm>/Y

表現型アノテーション

MGI marker

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

• porcupine homolog (Drosophila)
  http://metadb.riken.jp/db/mgi_rdf/MGI:1890212

遺伝子型

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

• Porcn<tm1.1Lcm>/Y

アレルシンボル

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

• Porcn<tm1.1Lcm>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * C57BL/6

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Jared J. Barrott, et.al., Deletion of mouse Porcn blocks Wnt ligand secretion and reveals an ectodermal etiology of human focal dermal hypoplasia/Goltz syndrome., Proceedings of the National Academy of Sciences of the United States of America, 2011, 108
  http://rdf.ncbi.nlm.nih.gov/pubmed/21768372