abnormal blood vessel physiology_Cul3<tm1.1Arte>/Cul3<+>

http://metadb.riken.jp/0000249IC57BL6JC57BL6NCul3tm11ArteCul3Cul3Cul3tm11Arte

abnormal blood vessel physiology_Cul3<tm1.1Arte>/Cul3<+>

表現型アノテーション

MGI marker

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

• cullin 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:1347360

遺伝子型

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

• Cul3<tm1.1Arte>/Cul3<+>

アレルシンボル

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

• Cul3<+>|Cul3<tm1.1Arte>

遺伝的背景

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

• involves: C57BL/6J * C57BL/6N

MP annotation

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

• abnormal blood vessel physiology
  http://purl.obolibrary.org/obo/MP_0000249

文献

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

• Frances-Rose. Schumacher, et.al., Characterisation of the Cullin-3 mutation that causes a severe form of familial hypertension and hyperkalaemia., EMBO molecular medicine, 2015, 7
  http://rdf.ncbi.nlm.nih.gov/pubmed/26286618