MGP Database

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MGP001866

Ontology/Pathway Information

Entrez Gene ID4124
Gene Namemannosidase, alpha, class 2A, member 1
Gene Symbol MAN2A1
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005801 IEA:EnsemblCcis-Golgi network
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0000139 TAS:ReactomeCGolgi membrane
GO:0016021 IEA:UniProtKB-KWCintegral component of membrane
GO:0016020 IDA:UniProtKBCmembrane
GO:0030246 IEA:InterProFcarbohydrate binding
GO:0016799 IEA:EnsemblFhydrolase activity, hydrolyzing N-glycosyl compounds
GO:0004572 TAS:ProtIncFmannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase activity
GO:0008270 IEA:InterProFzinc ion binding
GO:0044267 TAS:ReactomePcellular protein metabolic process
GO:0001701 IEA:EnsemblPin utero embryonic development
GO:0001889 IEA:EnsemblPliver development
GO:0048286 IEA:EnsemblPlung alveolus development
GO:0006013 IEA:InterProPmannose metabolic process
GO:0007005 IEA:EnsemblPmitochondrion organization
GO:0006491 IEA:EnsemblPN-glycan processing
GO:0050769 IEA:EnsemblPpositive regulation of neurogenesis
GO:0043687 TAS:ReactomePpost-translational protein modification
GO:0018279 TAS:ReactomePprotein N-linked glycosylation via asparagine
GO:0007585 IEA:EnsemblPrespiratory gaseous exchange
GO:0060042 IEA:EnsemblPretina morphogenesis in camera-type eye
GO:0007033 IEA:EnsemblPvacuole organization
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_22426Asparagine N-linked glycosylation
REACT_268132Defective ALG11 causes ALG11-CDG (CDG-1p)
REACT_267773Defective ALG12 causes ALG12-CDG (CDG-1g)
REACT_268645Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS)
REACT_268144Defective ALG1 causes ALG1-CDG (CDG-1k)
REACT_268833Defective ALG2 causes ALG2-CDG (CDG-1i)
REACT_268185Defective ALG3 causes ALG3-CDG (CDG-1d)
REACT_267765Defective ALG6 causes ALG6-CDG (CDG-1c)
REACT_268459Defective ALG8 causes ALG8-CDG (CDG-1h)
REACT_268015Defective ALG9 causes ALG9-CDG (CDG-1l)
REACT_268438Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
REACT_268849Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2
REACT_268813Defective MAN1B1 causes MRT15
REACT_268600Defective MGAT2 causes MGAT2-CDG (CDG-2a)
REACT_267905Defective MOGS causes MOGS-CDG (CDG-2b)
REACT_268619Defective MPDU1 causes MPDU1-CDG (CDG-1f)
REACT_268458Defective RFT1 causes RFT1-CDG (CDG-1n)
REACT_116125Disease
REACT_267875Diseases associated with N-glycosylation of proteins
REACT_268324Diseases of glycosylation
REACT_17015Metabolism of proteins
REACT_25208N-glycan antennae elongation in the medial/trans-Golgi
REACT_22161Post-translational protein modification
REACT_25302Reactions specific to the complex N-glycan synthesis pathway
REACT_25046Transport to the Golgi and subsequent modification
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