RAB1B
Ras-related protein Rab-1B
Also known as: RAB1B_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H0U4
- Gene
- RAB1B
- Ensembl
- ENSG00000174903
- Chromosome
- 11
- Canonical length
- 201 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Endoplasmic reticulum,Golgi apparatus
OverviewNCBI Gene
Members of the RAB protein family, such as RAB1B, are low molecular mass monomeric GTPases localized on the cytoplasmic surfaces of distinct membrane-bound organelles. RAB1B functions in the early secretory pathway and is essential for vesicle transport between the endoplasmic reticulum (ER) and Golgi (Chen et al., 1997 [PubMed 9030196]; Alvarez et al., 2003 [PubMed 12802079]).[supplied by OMIM, Jan 2009]
Canonical amino-acid sequenceUniProt
201 residues, UniProt reviewed canonical sequence.
>Q9H0U4|RAB1B
1 MNPEYDYLFK LLLIGDSGVG KSCLLLRFAD DTYTESYIST IGVDFKIRTI ELDGKTIKLQ
61 IWDTAGQERF RTITSSYYRG AHGIIVVYDV TDQESYANVK QWLQEIDRYA SENVNKLLVG
121 NKSDLTTKKV VDNTTAKEFA DSLGIPFLET SAKNATNVEQ AFMTMAAEIK KRMGPGAASG
181 GERPNLKIDS TPVKPAGGGC CLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RAB1B 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)
- 0.31
- Highest tissue expression
- 242 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 242 nTPM
- esophagus: 188 nTPM
- blood vessel: 152 nTPM
- heart muscle: 151 nTPM
- skin: 151 nTPM
- prostate: 144 nTPM
Single-cell type
- platelets: 411 nCPM
- esophageal apical cells: 213 nCPM
- esophageal suprabasal cells: 128 nCPM
- megakaryocytes: 118 nCPM
- extravillous trophoblasts: 102 nCPM
- colonocytes: 97 nCPM
Immune cell
- neutrophil: 422 nTPM
- total PBMC: 375 nTPM
- eosinophil: 330 nTPM
- non-classical monocyte: 245 nTPM
- gdT-cell: 228 nTPM
- intermediate monocyte: 212 nTPM
Brain region
- thalamus: 137 nTPM
- medulla oblongata: 132 nTPM
- midbrain: 129 nTPM
- amygdala: 128 nTPM
- spinal cord: 125 nTPM
- pons: 125 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)
- 0.42
- gnomAD pLI
- 0.88
- gnomAD missense Z
- 1.74
- DepMap mean gene effect
- -0.44
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- autophagosome assembly
- endoplasmic reticulum to Golgi vesicle-mediated transport
- Golgi organization
- intracellular protein transport
- positive regulation of glycoprotein metabolic process
- regulation of autophagosome assembly
- virion assembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RAB1B 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 RAB1B as an antibody target. Whether an autoantibody or antibody against RAB1B could matter depends on whether native RAB1B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RAB1B 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 RAB1B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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