about
P688
Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver diseaseRadixin deficiency causes conjugated hyperbilirubinemia with loss of Mrp2 from bile canalicular membranesHepatocyte nuclear factor-1alpha is an essential regulator of bile acid and plasma cholesterol metabolismFibrates induce mdr2 gene expression and biliary phospholipid secretion in the mouseFunctional analysis of chimeric genes obtained by exchanging homologous domains of the mouse mdr1 and mdr2 genes
P921
description
mammalian protein found in Mus musculus
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in ATP-binding cassette, sub-family B (MDR/TAP), member 4
@nl
protèin
@ace
protéine
@fr
بروتين في فأر المنازل
@ar
name
ATP-binding cassette, sub-family B (MDR/TAP), member 4
@en
ATP-binding cassette, sub-family B (MDR/TAP), member 4
@nl
type
label
ATP-binding cassette, sub-family B (MDR/TAP), member 4
@en
ATP-binding cassette, sub-family B (MDR/TAP), member 4
@nl
altLabel
3.6.3.44
@en
ATP-binding cassette sub-family B member 4
@en
Abcb4
@en
P glycoprotein 2
@en
P-glycoprotein 2
@en
P-glycoprotein 3
@en
multidrug resistance protein 2
@en
multidrug resistance protein 3
@en
phosphatidylcholine translocator ABCB4
@en
prefLabel
ATP-binding cassette, sub-family B (MDR/TAP), member 4
@en
ATP-binding cassette, sub-family B (MDR/TAP), member 4
@nl
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ENSMUSP00000003717
ENSMUSP00000142425