no abnormal phenotype detected_Epor<tm1.3Jtp>/Epor<+>

http://metadb.riken.jp/0002169I129P2OlaHsdC57BL6Eportm13JtpEporEportm13JtpEpor

no abnormal phenotype detected_Epor<tm1.3Jtp>/Epor<+>

表現型アノテーション

MGI marker

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

• erythropoietin receptor
  http://metadb.riken.jp/db/mgi_rdf/MGI:95408

遺伝子型

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

• Epor<tm1.3Jtp>/Epor<+>

アレルシンボル

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

• Epor<tm1.3Jtp>|Epor<+>

遺伝的背景

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

• involves: 129P2/OlaHsd * 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

• V. Divoky, et.al., Mouse model of congenital polycythemia: Homologous replacement of murine gene by mutant human erythropoietin receptor gene., Proceedings of the National Academy of Sciences of the United States of America, 2001, 98
  http://rdf.ncbi.nlm.nih.gov/pubmed/11158582