no abnormal phenotype detected_Urod<tm1Kush>/Urod<+>

http://metadb.riken.jp/0002169I129S1Sv129X1SvJUrodtm1KushUrodUrodUrodtm1Kush

no abnormal phenotype detected_Urod<tm1Kush>/Urod<+>

表現型アノテーション

MGI marker

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

• uroporphyrinogen decarboxylase
  http://metadb.riken.jp/db/mgi_rdf/MGI:98916

遺伝子型

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

• Urod<tm1Kush>/Urod<+>

アレルシンボル

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

• Urod<+>|Urod<tm1Kush>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ

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

• J D. Phillips, et.al., A mouse model of familial porphyria cutanea tarda., Proceedings of the National Academy of Sciences of the United States of America, 2001, 98
  http://rdf.ncbi.nlm.nih.gov/pubmed/11134514