MON1B
Vacuolar fusion protein MON1 homolog B
Also known as: HSRG1, KIAA0872, MON1B_HUMAN, SAND2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7L1V2
- Gene
- MON1B
- Ensembl
- ENSG00000103111
- Chromosome
- 16
- Canonical length
- 547 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Involved in early viral transcription and late viral transcription. Located in cytoplasm. Part of Mon1-Ccz1 complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
547 residues, UniProt reviewed canonical sequence.
>Q7L1V2|MON1B
1 MEVGGDTAAP APGGAEDLED TQFPSEEARE GGGVHAVPPD PEDEGLEETG SKDKDQPPSP
61 SPPPQSEALS STSRLWSPAA PENSPTCSPE SSSGGQGGDP SDEEWRSQRK HVFVLSEAGK
121 PIYSRYGSVE ALSATMGVMT ALVSFVQSAG DAIRAIYAED HKLVFLQQGP LLLVAMSRTS
181 QSAAQLRGEL LAVHAQIVST LTRASVARIF AHKQNYDLRR LLAGSERTLD RLLDSMEQDP
241 GALLLGAVRC VPLARPLRDA LGALLRRCTA PGLALSVLAV GGRLITAAQE RNVLAECRLD
301 PADLQLLLDW VGAPAFAAGE AWAPVCLPRF NPDGFFYAYV ARLDAMPVCL LLLGTQREAF
361 HAMAACRRLV EDGMHALGAM RALGEAASFS NASSASAPAY SVQAVGAPGL RHFLYKPLDI
421 PDHHRQLPQF TSPELEAPYS REEERQRLSD LYHRLHARLH STSRPLRLIY HVAEKETLLA
481 WVTSKFELYT CLSPLVTKAG AILVVTKLLR WVKKEEDRLF IRYPPKYSTP PATSTDQAAH
541 NGLFTGLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MON1B 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 19 nTPM
Expression across tissuesHPA
Tissue
- retina: 19 nTPM
- spinal cord: 19 nTPM
- prostate: 19 nTPM
- thyroid gland: 18 nTPM
- lymph node: 17 nTPM
- midbrain: 17 nTPM
Single-cell type
- neutrophils: 29 nCPM
- early spermatids: 22 nCPM
- prostatic glandular cells: 20 nCPM
- cone photoreceptor cells: 19 nCPM
- late spermatids: 18 nCPM
- breast lactating cells: 16 nCPM
Immune cell
- neutrophil: 22 nTPM
- basophil: 18 nTPM
- eosinophil: 17 nTPM
- intermediate monocyte: 16 nTPM
- non-classical monocyte: 11 nTPM
- NK-cell: 10 nTPM
Brain region
- basal ganglia: 54 nTPM
- medulla oblongata: 53 nTPM
- midbrain: 51 nTPM
- thalamus: 49 nTPM
- white matter: 47 nTPM
- pons: 46 nTPM
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)
- 0.6
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 0.85
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- early viral transcription
- late viral transcription
- protein targeting to vacuole
- vesicle-mediated transport
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MON1B 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 MON1B as an antibody target. Whether an autoantibody or antibody against MON1B could matter depends on whether native MON1B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MON1B 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 MON1B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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