no abnormal phenotype detected_Hmbs<tm2Uam>/Hmbs<tm2Uam>

http://metadb.riken.jp/0002169C57BL6Hmbstm2UamHmbstm2UamHmbstm2UamHmbstm2Uam

no abnormal phenotype detected_Hmbs<tm2Uam>/Hmbs<tm2Uam>

表現型アノテーション

MGI marker

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

• hydroxymethylbilane synthase
  http://metadb.riken.jp/db/mgi_rdf/MGI:96112

遺伝子型

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

• Hmbs<tm2Uam>/Hmbs<tm2Uam>

アレルシンボル

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

• Hmbs<tm2Uam>

遺伝的背景

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

• C57BL/6-Hmbs<tm2Uam>

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

• R L. Lindberg, et.al., Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyria., Nature genetics, 1996, 12
  http://rdf.ncbi.nlm.nih.gov/pubmed/8563760