abnormal circulating alanine transaminase level_Abcb4<tm1Bor>/Abcb4<tm1Bor>

http://metadb.riken.jp/0001573EI129P2OlaHsdorI129P2OlaHsdFVBNAbcb4tm1BorAbcb4tm1BorAbcb4tm1Bor

abnormal circulating alanine transaminase level_Abcb4<tm1Bor>/Abcb4<tm1Bor>

表現型アノテーション

MGI marker

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

• ATP-binding cassette, sub-family B (MDR/TAP), member 4
  http://metadb.riken.jp/db/mgi_rdf/MGI:97569

遺伝子型

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

• Abcb4<tm1Bor>/Abcb4<tm1Bor>

アレルシンボル

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

• Abcb4<tm1Bor>

遺伝的背景

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

• either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * FVB/N)

MP annotation

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

• abnormal circulating alanine transaminase level
  http://purl.obolibrary.org/obo/MP_0001573

文献

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

• J J. Smit, et.al., Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease., Cell, 1993, 75
  http://rdf.ncbi.nlm.nih.gov/pubmed/8106172