abnormal embryo development_Wdr35<tm2a(EUCOMM)Hmgu>/Wdr35<yeti>

http://metadb.riken.jp/0001672IC57BL6NWdr35tm2aEUCOMMHmguWdr35yetiWdr35tm2aEUCOMMHmguWdr35yeti

abnormal embryo development_Wdr35<tm2a(EUCOMM)Hmgu>/Wdr35<yeti>

表現型アノテーション

MGI marker

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

• WD repeat domain 35
  http://metadb.riken.jp/db/mgi_rdf/MGI:1921932

遺伝子型

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

• Wdr35<tm2a(EUCOMM)Hmgu>/Wdr35<yeti>

アレルシンボル

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

• Wdr35<tm2a(EUCOMM)Hmgu>|Wdr35<yeti>

遺伝的背景

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

• involves: C57BL/6N

MP annotation

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

• abnormal embryogenesis/ development
  http://purl.obolibrary.org/obo/MP_0001672

文献

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

• Pleasantine. Mill, et.al., Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis., American journal of human genetics, 2011, 88
  http://rdf.ncbi.nlm.nih.gov/pubmed/21473986