no abnormal phenotype detected_Wisp3<tm2Mawa>/Wisp3<tm2Mawa>

http://metadb.riken.jp/0002169129SSvEvWisp3tm2MawaWisp3tm2MawaWisp3tm2MawaWisp3tm2Mawa

no abnormal phenotype detected_Wisp3<tm2Mawa>/Wisp3<tm2Mawa>

表現型アノテーション

MGI marker

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

• WNT1 inducible signaling pathway protein 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:2685581

遺伝子型

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

• Wisp3<tm2Mawa>/Wisp3<tm2Mawa>

アレルシンボル

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

• Wisp3<tm2Mawa>

遺伝的背景

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

• 129S/SvEv-Wisp3<tm2Mawa>

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

• Wendy E. Kutz, et.al., WISP3, the gene responsible for the human skeletal disease progressive pseudorheumatoid dysplasia, is not essential for skeletal function in mice., Molecular and cellular biology, 2005, 25
  http://rdf.ncbi.nlm.nih.gov/pubmed/15601861