RAB40B
Ras-related protein Rab-40B
Also known as: RAR, RB40B_HUMAN, SEC4L
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q12829
- Gene
- RAB40B
- Ensembl
- ENSG00000141542
- Chromosome
- 17
- Canonical length
- 278 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
The protein encoded by this gene has similarity to a yeast protein which suggests a role of the gene product in regulating secretory vesicles. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
278 residues, UniProt reviewed canonical sequence.
>Q12829|RAB40B
1 MSALGSPVRA YDFLLKFLLV GDSDVGKGEI LASLQDGAAE SPYGHPAGID YKTTTILLDG
61 RRVKLQLWDT SGQGRFCTIF RSYSRGAQGV ILVYDIANRW SFDGIDRWIK EIDEHAPGVP
121 KILVGNRLHL AFKRQVPTEQ AQAYAERLGV TFFEVSPLCN FNITESFTEL ARIVLLRHGM
181 DRLWRPSKVL SLQDLCCRAV VSCTPVHLVD KLPLPIALRS HLKSFSMANG LNARMMHGGS
241 YSLTTSSTHK RSSLRKVKLV RPPQSPPKNC TRNSCKISLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RAB40B 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 106 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 106 nTPM
- spinal cord: 85 nTPM
- amygdala: 74 nTPM
- hippocampal formation: 70 nTPM
- midbrain: 60 nTPM
- cerebral cortex: 56 nTPM
Single-cell type
- oligodendrocytes: 185 nCPM
- endometrial glandular cells: 142 nCPM
- epididymal clear cells: 131 nCPM
- endometrial luminal cells: 124 nCPM
- urothelial cells: 101 nCPM
- colonocytes: 78 nCPM
Immune cell
- plasmacytoid DC: 6.5 nTPM
- non-classical monocyte: 3.4 nTPM
- memory B-cell: 2.8 nTPM
- NK-cell: 2 nTPM
- T-reg: 1.8 nTPM
- memory CD8 T-cell: 1.6 nTPM
Brain region
- white matter: 107 nTPM
- basal ganglia: 85 nTPM
- cerebral cortex: 81 nTPM
- medulla oblongata: 77 nTPM
- midbrain: 69 nTPM
- amygdala: 65 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)
- 1.34
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.46
- DepMap mean gene effect
- -0.02
- 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
- cellular detoxification
- exocytosis
- intracellular signal transduction
- negative regulation of actin filament bundle assembly
- positive regulation of cell migration
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein ubiquitination
- regulation of lamellipodium organization
Molecular functions
- G protein activity
- GTP binding
- GTPase activity
- metal ion binding
- ubiquitin-like ligase-substrate adaptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RAB40B 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 RAB40B as an antibody target. Whether an autoantibody or antibody against RAB40B could matter depends on whether native RAB40B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RAB40B is annotated at the cell surface, where native RAB40B is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label RAB40B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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