MAN2A2
Alpha-mannosidase 2x
Also known as: HsT19662, MA2A2_HUMAN, MANA2X
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P49641
- Gene
- MAN2A2
- Ensembl
- ENSG00000196547
- Chromosome
- 15
- Canonical length
- 1150 aa
- Protein class
- Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Cytoplasmic bodies
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Predicted to enable alpha-mannosidase activity. Predicted to be involved in N-glycan processing. Predicted to be located in Golgi apparatus and membrane. Predicted to be active in Golgi membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1150 residues, UniProt reviewed canonical sequence.
>P49641|MAN2A2
1 MKLKKQVTVC GAAIFCVAVF SLYLMLDRVQ HDPTRHQNGG NFPRSQISVL QNRIEQLEQL
61 LEENHEIISH IKDSVLELTA NAEGPPAMLP YYTVNGSWVV PPEPRPSFFS ISPQDCQFAL
121 GGRGQKPELQ MLTVSEELPF DNVDGGVWRQ GFDISYDPHD WDAEDLQVFV VPHSHNDPGW
181 IKTFDKYYTE QTQHILNSMV SKLQEDPRRR FLWAEVSFFA KWWDNINVQK RAAVRRLVGN
241 GQLEIATGGW VMPDEANSHY FALIDQLIEG HQWLERNLGA TPRSGWAVDP FGYSSTMPYL
301 LRRANLTSML IQRVHYAIKK HFAATHSLEF MWRQTWDSDS STDIFCHMMP FYSYDVPHTC
361 GPDPKICCQF DFKRLPGGRI NCPWKVPPRA ITEANVAERA ALLLDQYRKK SQLFRSNVLL
421 VPLGDDFRYD KPQEWDAQFF NYQRLFDFFN SRPNLHVQAQ FGTLSDYFDA LYKRTGVEPG
481 ARPPGFPVLS GDFFSYADRE DHYWTGYYTS RPFYKSLDRV LEAHLRGAEV LYSLAAAHAR
541 RSGLAGRYPL SDFTLLTEAR RTLGLFQHHD AITGTAKEAV VVDYGVRLLR SLVNLKQVII
601 HAAHYLVLGD KETYHFDPEA PFLQVDDTRL SHDALPERTV IQLDSSPRFV VLFNPLEQER
661 FSMVSLLVNS PRVRVLSEEG QPLAVQISAH WSSATEAVPD VYQVSVPVRL PALGLGVLQL
721 QLGLDGHRTL PSSVRIYLHG RQLSVSRHEA FPLRVIDSGT SDFALSNRYM QVWFSGLTGL
781 LKSIRRVDEE HEQQVDMQVL VYGTRTSKDK SGAYLFLPDG EAKPYVPKEP PVLRVTEGPF
841 FSEVVAYYEH IHQAVRLYNL PGVEGLSLDI SSLVDIRDYV NKELALHIHT DIDSQGIFFT
901 DLNGFQVQPR RYLKKLPLQA NFYPMPVMAY IQDAQKRLTL HTAQALGVSS LKDGQLEVIL
961 DRRLMQDDNR GLGQGLKDNK RTCNRFRLLL ERRTVGSEVQ DSHSTSYPSL LSHLTSMYLN
1021 APALALPVAR MQLPGPGLRS FHPLASSLPC DFHLLNLRTL QAEEDTLPSA ETALILHRKG
1081 FDCGLEAKNL GFNCTTSQGK VALGSLFHGL DVVFLQPTSL TLLYPLASPS NSTDVYLEPM
1141 EIATFRLRLGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MAN2A2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.21
- Highest tissue expression
- 74 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 74 nTPM
- retina: 70 nTPM
- skeletal muscle: 65 nTPM
- cerebellum: 54 nTPM
- spinal cord: 53 nTPM
- pancreas: 46 nTPM
Single-cell type
- neutrophils: 213 nCPM
- platelets: 128 nCPM
- oligodendrocytes: 107 nCPM
- erythrocyte progenitors: 83 nCPM
- megakaryocyte-erythroid progenitors: 74 nCPM
- myonuclei: 65 nCPM
Immune cell
- basophil: 8.8 nTPM
- neutrophil: 8 nTPM
- non-classical monocyte: 3 nTPM
- plasmacytoid DC: 1.6 nTPM
- total PBMC: 1.4 nTPM
- classical monocyte: 1.2 nTPM
Brain region
- white matter: 189 nTPM
- pons: 129 nTPM
- medulla oblongata: 128 nTPM
- basal ganglia: 128 nTPM
- thalamus: 120 nTPM
- midbrain: 118 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about MAN2A2.
Disease | GeneticClinVar
2 pathogenic / likely-pathogenic of 221 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.62
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.05
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
- alpha-mannosidase activity
- carbohydrate binding
- hydrolase activity, hydrolyzing N-glycosyl compounds
- mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase activity
- metal ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Glycoside hydrolase family 38, N-terminal domain
- Galactose mutarotase-like domain superfamily
- Glycoside hydrolase/deacetylase, beta/alpha-barrel
- Glycosyl hydrolase family 38, C-terminal
- Glycosyl hydrolase, all-beta
- Glycoside hydrolase family 38, central domain
- Glycoside hydrolase 38, N-terminal domain superfamily
- Glycoside hydrolase families 57/38, central domain superfamily
- Glycoside hydrolase family 38, central domain superfamily
- Glycosyl Hydrolase Family 38
- Glycosyl hydrolases family 38 N-terminal domain
- Glycosyl hydrolases family 38 C-terminal domain
- Alpha mannosidase middle domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MAN2A2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MAN2A2 as an antibody target. Whether an autoantibody or antibody against MAN2A2 could matter depends on whether native MAN2A2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MAN2A2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label MAN2A2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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