LMPD Database

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LMP012554

Gene Information

Entrez Gene ID25732
Gene Nameacid phosphatase 5, tartrate resistant
Gene SymbolAcp5
SpeciesRattus norvegicus
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005615 IDA:RGDCextracellular space
GO:0016021 TAS:RGDCintegral component of membrane
GO:0005764 TAS:RGDClysosome
GO:0003993 IDA:RGDFacid phosphatase activity
GO:0008199 ISS:UniProtKBFferric iron binding
GO:0008198 ISS:UniProtKBFferrous iron binding
GO:0016787 IDA:RGDFhydrolase activity
GO:0045453 IEP:RGDPbone resorption
GO:0016311 IDA:GOCPdephosphorylation
GO:0008152 IDA:GOCPmetabolic process
GO:0033555 IEP:RGDPmulticellular organismal response to stress
GO:0007162 IDA:RGDPnegative regulation of cell adhesion
GO:0001503 IEP:RGDPossification
GO:0030316 IEP:RGDPosteoclast differentiation
GO:0030335 IMP:RGDPpositive regulation of cell migration
GO:0070723 IEP:RGDPresponse to cholesterol
GO:0033591 IEP:RGDPresponse to L-ascorbic acid
GO:0014070 IEP:RGDPresponse to organic cyclic compound
GO:0010043 IEP:RGDPresponse to zinc ion
KEGG Pathway Links
KEGG Pathway IDDescription
ko04142Lysosome
rno04142Lysosome
ko04380Osteoclast differentiation
rno04380Osteoclast differentiation
ko05323Rheumatoid arthritis
rno05323Rheumatoid arthritis
ko00740Riboflavin metabolism
rno00740Riboflavin metabolism
REACTOME Pathway Links
REACTOME Pathway IDDescription
5953298Defective AMN causes hereditary megaloblastic anemia 1
5953308Defective BTD causes biotidinase deficiency
5953307Defective CD320 causes methylmalonic aciduria
5953299Defective CUBN causes hereditary megaloblastic anemia 1
5953296Defective GIF causes intrinsic factor deficiency
5953310Defective HLCS causes multiple carboxylase deficiency
5953297Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
5953305Defective MMAA causes methylmalonic aciduria type cblA
5953302Defective MMAB causes methylmalonic aciduria type cblB
5953304Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
5953303Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
5953301Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
5953300Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
5953306Defective MUT causes methylmalonic aciduria mut type
5953293Defective TCN2 causes hereditary megaloblastic anemia
5953309Defects in biotin (Btn) metabolism
5953294Defects in cobalamin (B12) metabolism
5953295Defects in vitamin and cofactor metabolism
5953253Disease
5953250Metabolism
5953292Metabolism of vitamins and cofactors
5953291Metabolism of water-soluble vitamins and cofactors
5953987Vitamin B2 (riboflavin) metabolism