RAB27B
Ras-related protein Rab-27B
Also known as: RB27B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O00194
- Gene
- RAB27B
- Ensembl
- ENSG00000041353
- Chromosome
- 18
- Canonical length
- 218 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Golgi apparatus,Plasma membrane,Cytosol
OverviewNCBI Gene
Enables guanyl ribonucleotide binding activity; myosin V binding activity; and protein domain specific binding activity. Involved in multivesicular body sorting pathway and positive regulation of exocytosis. Located in Golgi stack and cytoplasmic vesicle. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
218 residues, UniProt reviewed canonical sequence.
>O00194|RAB27B
1 MTDGDYDYLI KLLALGDSGV GKTTFLYRYT DNKFNPKFIT TVGIDFREKR VVYNAQGPNG
61 SSGKAFKVHL QLWDTAGQER FRSLTTAFFR DAMGFLLMFD LTSQQSFLNV RNWMSQLQAN
121 AYCENPDIVL IGNKADLPDQ REVNERQARE LADKYGIPYF ETSAATGQNV EKAVETLLDL
181 IMKRMEQCVE KTQIPDTVNG GNSGNLDGEK PPEKKCICLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RAB27B 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)
- 0.32
- Highest tissue expression
- 42 nTPM
Expression across tissuesHPA
Tissue
- stomach: 42 nTPM
- prostate: 19 nTPM
- skin: 15 nTPM
- cerebral cortex: 14 nTPM
- salivary gland: 13 nTPM
- esophagus: 13 nTPM
Single-cell type
- platelets: 1,214 nCPM
- megakaryocytes: 933 nCPM
- mast cells: 618 nCPM
- foveolar cells: 567 nCPM
- megakaryocyte progenitors: 377 nCPM
- esophageal apical cells: 306 nCPM
Immune cell
- NK-cell: 2.6 nTPM
- gdT-cell: 2.2 nTPM
- total PBMC: 1.6 nTPM
- memory CD8 T-cell: 1.1 nTPM
- naive CD8 T-cell: 1 nTPM
- memory CD4 T-cell: 0.7 nTPM
Brain region
- cerebral cortex: 46 nTPM
- basal ganglia: 38 nTPM
- hypothalamus: 30 nTPM
- white matter: 26 nTPM
- thalamus: 22 nTPM
- hippocampal formation: 22 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)
- 0.86
- gnomAD pLI
- 0.04
- gnomAD missense Z
- 0.18
- DepMap mean gene effect
- 0.12
- 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
- anterograde axonal protein transport
- exocytosis
- multivesicular body sorting pathway
- positive regulation of exocytosis
- synaptic vesicle endocytosis
Molecular functions
- G protein activity
- GDP binding
- GTP binding
- GTPase activity
- myosin V binding
- protein domain specific binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RAB27B 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 RAB27B as an antibody target. Whether an autoantibody or antibody against RAB27B could matter depends on whether native RAB27B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RAB27B 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 RAB27B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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