RABL3
Rab-like protein 3
Also known as: MGC23920, RABL3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5HYI8
- Gene
- RABL3
- Ensembl
- ENSG00000144840
- Chromosome
- 3
- Canonical length
- 236 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Endoplasmic reticulum
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Predicted to enable GTP binding activity; GTPase activity; and protein homodimerization activity. Involved in regulation of Ras protein signal transduction and regulation of protein lipidation. Predicted to be active in endomembrane system. Implicated in pancreatic cancer. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
236 residues, UniProt reviewed canonical sequence.
>Q5HYI8|RABL3
1 MASLDRVKVL VLGDSGVGKS SLVHLLCQNQ VLGNPSWTVG CSVDVRVHDY KEGTPEEKTY
61 YIELWDVGGS VGSASSVKST RAVFYNSVNG IIFVHDLTNK KSSQNLRRWS LEALNRDLVP
121 TGVLVTNGDY DQEQFADNQI PLLVIGTKLD QIHETKRHEV LTRTAFLAED FNPEEINLDC
181 TNPRYLAAGS SNAVKLSRFF DKVIEKRYFL REGNQIPGFP DRKRFGAGTL KSLHYDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RABL3 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)
- 0.35
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 12 nTPM
- parathyroid gland: 11 nTPM
- tongue: 11 nTPM
- adipose tissue: 10 nTPM
- kidney: 9.2 nTPM
- liver: 9.1 nTPM
Single-cell type
- cone photoreceptor cells: 201 nCPM
- retinal bipolar cells: 61 nCPM
- late primary spermatocytes: 58 nCPM
- adrenal cortex cells: 50 nCPM
- endometrial ciliated cells: 49 nCPM
- esophageal apical cells: 46 nCPM
Immune cell
- myeloid DC: 6.6 nTPM
- NK-cell: 5.7 nTPM
- intermediate monocyte: 5.6 nTPM
- T-reg: 5.3 nTPM
- memory CD8 T-cell: 5.1 nTPM
- gdT-cell: 4.6 nTPM
Brain region
- white matter: 8.1 nTPM
- medulla oblongata: 6.9 nTPM
- hypothalamus: 6.7 nTPM
- midbrain: 6.1 nTPM
- spinal cord: 6 nTPM
- cerebellum: 5.6 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about RABL3.
Disease | AllUniProt
Conditions RABL3 is implicated in, by any mechanism.
- Pancreatic cancer 5 (PNCA5) MIM:618680
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)
- 0.97
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.43
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- B cell differentiation
- intracellular protein transport
- natural killer cell differentiation
- positive regulation of cilium assembly
- protein stabilization
- regulation of Ras protein signal transduction
- T cell differentiation in thymus
- regulation of protein lipidation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RABL3 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 RABL3 as an antibody target. Whether an autoantibody or antibody against RABL3 could matter depends on whether native RABL3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RABL3 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 RABL3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...