no abnormal phenotype detected_Wdfy3<tm1c(KOMP)Mbp>/Wdfy3<tm1c(KOMP)Mbp>

http://metadb.riken.jp/0002169C57BL6NWdfy3tm1cKOMPMbpWdfy3tm1cKOMPMbpWdfy3tm1cKOMPMbpWdfy3tm1cKOMPMbp

no abnormal phenotype detected_Wdfy3<tm1c(KOMP)Mbp>/Wdfy3<tm1c(KOMP)Mbp>

表現型アノテーション

MGI marker

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

• WD repeat and FYVE domain containing 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:1096875

遺伝子型

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

• Wdfy3<tm1c(KOMP)Mbp>/Wdfy3<tm1c(KOMP)Mbp>

アレルシンボル

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

• Wdfy3<tm1c(KOMP)Mbp>

遺伝的背景

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

• C57BL/6N-Wdfy3<tm1c(KOMP)Mbp>

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

• Lori A. Orosco, et.al., Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology., Nature communications, 2014, 5
  http://rdf.ncbi.nlm.nih.gov/pubmed/25198012