abnormal oogenesis_Prlr<tm1Cnp>/Prlr<tm1Cnp>

http://metadb.riken.jp/0001931EI129Sv129P2OlaHsdorI129P2OlaHsdC57BL6Prlrtm1CnpPrlrtm1CnpPrlrtm1Cnp

abnormal oogenesis_Prlr<tm1Cnp>/Prlr<tm1Cnp>

表現型アノテーション

MGI marker

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

• prolactin receptor
  http://metadb.riken.jp/db/mgi_rdf/MGI:97763

遺伝子型

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

• Prlr<tm1Cnp>/Prlr<tm1Cnp>

アレルシンボル

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

• Prlr<tm1Cnp>

遺伝的背景

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

• either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)

MP annotation

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

• abnormal oogenesis
  http://purl.obolibrary.org/obo/MP_0001931

文献

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

• C J. Ormandy, et.al., Null mutation of the prolactin receptor gene produces multiple reproductive defects in the mouse., Genes & development, 1997, 11
  http://rdf.ncbi.nlm.nih.gov/pubmed/9009200