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General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.
Gene namei
Official gene symbol, which is typically a short form of the gene name, according to HGNC.
ER degradation enhancing alpha-mannosidase like protein 3
Protein classi
Assigned HPA protein class(es) for the encoded protein(s).
Disease related genes Enzymes Human disease related genes Potential drug targets
Predicted locationi
All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.
Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.
Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).
The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.
Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.
Chromosome
1
Cytoband
q25.3
Chromosome location (bp)
184690237 - 184754907
Number of transcriptsi
Number of protein-coding transcripts from the gene as defined by Ensembl.
Useful information about the protein provided by UniProt.
Involved in endoplasmic reticulum-associated degradation (ERAD). Accelerates the glycoprotein ERAD by proteasomes, by catalyzing mannose trimming from Man8GlcNAc2 to Man7GlcNAc2 in the N-glycans 1. May also participate in mannose trimming from all glycoproteins and not just misfolded ones targeted to ERAD 2. May have alpha 1,2-mannosidase activity (By similarity)....show less
Molecular function (UniProt)i
Keywords assigned by UniProt to proteins due to their particular molecular function.
Hydrolase
Biological process (UniProt)i
Keywords assigned by UniProt to proteins because they are involved in a particular biological process.
Unfolded protein response
Ligand (UniProt)i
Keywords assigned by UniProt to proteins because they bind, are associated with, or whose activity is dependent of some molecule.
The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.
The Splice variant identifier links to the Ensembl website protein summary for the selected splice variant. The data in the Swissprot and TrEMBL columns links to corresponding pages in the UniProt database.
The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.
The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide and number of predicted transmembrane region(s) according to in-house majority decision methods based on sets of predictors are also reported.
Q9BZQ6 [Direct mapping] ER degradation-enhancing alpha-mannosidase-like protein 3
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Enzymes ENZYME proteins Hydrolases MEMSAT3 predicted membrane proteins Secreted proteins predicted by MDSEC SignalP predicted secreted proteins Phobius predicted secreted proteins SPOCTOPUS predicted secreted proteins DeepTMHMM predicted secreted proteins Predicted intracellular proteins Disease related genes Potential drug targets Human disease related genes Congenital disorders of metabolism Congenital disorders of glycan/glycoprotein metabolism Mapped to neXtProt neXtProt - Evidence at protein level Protein evidence (Kim et al 2014) Protein evidence (Ezkurdia et al 2014)
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GO:0004559[alpha-mannosidase activity] GO:0004571[mannosyl-oligosaccharide 1,2-alpha-mannosidase activity] GO:0005509[calcium ion binding] GO:0005783[endoplasmic reticulum] GO:0005788[endoplasmic reticulum lumen] GO:0005975[carbohydrate metabolic process] GO:0006486[protein glycosylation] GO:0006986[response to unfolded protein] GO:0016020[membrane] GO:0016787[hydrolase activity] GO:0036508[protein alpha-1,2-demannosylation] GO:0044322[endoplasmic reticulum quality control compartment] GO:0046872[metal ion binding] GO:1904380[endoplasmic reticulum mannose trimming] GO:1904382[mannose trimming involved in glycoprotein ERAD pathway]
Predicted intracellular proteins Intracellular proteins predicted by MDM and MDSEC Human disease related genes Congenital disorders of metabolism Congenital disorders of glycan/glycoprotein metabolism Protein evidence (Ezkurdia et al 2014)
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GO:0004571[mannosyl-oligosaccharide 1,2-alpha-mannosidase activity] GO:0005509[calcium ion binding] GO:0005783[endoplasmic reticulum] GO:0005975[carbohydrate metabolic process] GO:0006986[response to unfolded protein] GO:0008152[metabolic process] GO:0016020[membrane] GO:0016787[hydrolase activity] GO:0016798[hydrolase activity, acting on glycosyl bonds] GO:0036508[protein alpha-1,2-demannosylation] GO:0044322[endoplasmic reticulum quality control compartment] GO:0046872[metal ion binding] GO:1904380[endoplasmic reticulum mannose trimming] GO:1904382[mannose trimming involved in glycoprotein ERAD pathway]
Predicted intracellular proteins Intracellular proteins predicted by MDM and MDSEC Human disease related genes Congenital disorders of metabolism Congenital disorders of glycan/glycoprotein metabolism Protein evidence (Ezkurdia et al 2014)
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GO:0004571[mannosyl-oligosaccharide 1,2-alpha-mannosidase activity] GO:0005509[calcium ion binding] GO:0005783[endoplasmic reticulum] GO:0005975[carbohydrate metabolic process] GO:0006986[response to unfolded protein] GO:0008152[metabolic process] GO:0016020[membrane] GO:0016787[hydrolase activity] GO:0016798[hydrolase activity, acting on glycosyl bonds] GO:0036508[protein alpha-1,2-demannosylation] GO:0044322[endoplasmic reticulum quality control compartment] GO:0046872[metal ion binding] GO:1904380[endoplasmic reticulum mannose trimming] GO:1904382[mannose trimming involved in glycoprotein ERAD pathway]
Predicted intracellular proteins Intracellular proteins predicted by MDM and MDSEC Human disease related genes Congenital disorders of metabolism Congenital disorders of glycan/glycoprotein metabolism Protein evidence (Ezkurdia et al 2014)
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GO:0004571[mannosyl-oligosaccharide 1,2-alpha-mannosidase activity] GO:0005509[calcium ion binding] GO:0005783[endoplasmic reticulum] GO:0005975[carbohydrate metabolic process] GO:0006986[response to unfolded protein] GO:0008152[metabolic process] GO:0016020[membrane] GO:0016787[hydrolase activity] GO:0016798[hydrolase activity, acting on glycosyl bonds] GO:0036508[protein alpha-1,2-demannosylation] GO:0044322[endoplasmic reticulum quality control compartment] GO:0046872[metal ion binding] GO:1904380[endoplasmic reticulum mannose trimming] GO:1904382[mannose trimming involved in glycoprotein ERAD pathway]
Predicted intracellular proteins Intracellular proteins predicted by MDM and MDSEC Human disease related genes Congenital disorders of metabolism Congenital disorders of glycan/glycoprotein metabolism Protein evidence (Ezkurdia et al 2014)
Show all
GO:0004571[mannosyl-oligosaccharide 1,2-alpha-mannosidase activity] GO:0005509[calcium ion binding] GO:0005783[endoplasmic reticulum] GO:0005975[carbohydrate metabolic process] GO:0006986[response to unfolded protein] GO:0008152[metabolic process] GO:0016020[membrane] GO:0016787[hydrolase activity] GO:0016798[hydrolase activity, acting on glycosyl bonds] GO:0036508[protein alpha-1,2-demannosylation] GO:0044322[endoplasmic reticulum quality control compartment] GO:0046872[metal ion binding] GO:1904380[endoplasmic reticulum mannose trimming] GO:1904382[mannose trimming involved in glycoprotein ERAD pathway]