LMPD Database

LMP008346

Gene Information

Entrez Gene ID181677
Gene NameProtein MRP-3
Gene Symbolmrp-3
SpeciesCaenorhabditis elegans
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0016021 IEA:InterProCintegral component of membrane
GO:0005524 IEA:UniProtKB-KWFATP binding
GO:0042626 IEA:InterProFATPase activity, coupled to transmembrane movement of substances
REACTOME Pathway Links
REACTOME Pathway IDDescription
5653155ABC-family proteins mediated transport
5652697Arachidonic acid metabolism
5652531Cobalamin (Cbl, vitamin B12) transport and metabolism
5652539Defective AMN causes hereditary megaloblastic anemia 1
5652549Defective BTD causes biotidinase deficiency
5652548Defective CD320 causes methylmalonic aciduria
5652540Defective CUBN causes hereditary megaloblastic anemia 1
5652537Defective GIF causes intrinsic factor deficiency
5652551Defective HLCS causes multiple carboxylase deficiency
5652538Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
5652546Defective MMAA causes methylmalonic aciduria type cblA
5652543Defective MMAB causes methylmalonic aciduria type cblB
5652545Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
5652544Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
5652542Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
5652541Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
5652547Defective MUT causes methylmalonic aciduria mut type
5652534Defective TCN2 causes hereditary megaloblastic anemia
5652550Defects in biotin (Btn) metabolism
5652535Defects in cobalamin (B12) metabolism
5652536Defects in vitamin and cofactor metabolism
5652494Disease
5652491Metabolism
5652530Metabolism of lipids and lipoproteins
5652533Metabolism of vitamins and cofactors
5652532Metabolism of water-soluble vitamins and cofactors
5653112Synthesis of Leukotrienes (LT) and Eoxins (EX)
5652506Transmembrane transport of small molecules