RABEP2
Rab GTPase-binding effector protein 2
Also known as: FLJ23282, FRA, RABE2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H5N1
- Gene
- RABEP2
- Ensembl
- ENSG00000177548
- Chromosome
- 16
- Canonical length
- 569 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Golgi apparatus,Vesicles,Cytosol
OverviewNCBI Gene
Predicted to enable GTPase activator activity and growth factor activity. Involved in regulation of cilium assembly. Located in Golgi apparatus; cytosol; and microtubule organizing center. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
569 residues, UniProt reviewed canonical sequence.
>Q9H5N1|RABEP2
1 MAAAAPVAAD DDERRRRPGA ALEDSRSQEG ANGEAESGEL SRLRAELAGA LAEMETMKAV
61 AEVSESTKAE AVAAVQRQCQ EEVASLQAIL KDSISSYEAQ ITALKQERQQ QQQDCEEKER
121 ELGRLKQLLS RAYPLDSLEK QMEKAHEDSE KLREIVLPME KEIEELKAKL LRAEELIQEI
181 QRRPRHAPSL HGSTELLPLS RDPSPPLEPL EELSGDGGPA AEAFAHNCDD SASISSFSLG
241 GGVGSSSSLP QSRQGLSPEQ EETASLVSTG TLVPEGIYLP PPGYQLVPDT QWEQLQTEGR
301 QLQKDLESVS RERDELQEGL RRSNEDCAKQ MQVLLAQVQN SEQLLRTLQG TVSQAQERVQ
361 LQMAELVTTH KCLHHEVKRL NEENQGLRAE QLPSSAPQGS QQEQGEEESL PSSVPELQQL
421 LCCTRQEARA RLQAQEHGAE RLRIEIVTLR EALEEETVAR ASLEGQLRVQ REETEVLEAS
481 LCSLRTEMER VQQEQSKAQL PDLLSEQRAK VLRLQAELET SEQVQRDFVR LSQALQVRLE
541 RIRQAETLEQ VRSIMDEAPL TDVRDIKDTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RABEP2 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)
- 0.53
- Highest tissue expression
- 49 nTPM
Expression across tissuesHPA
Tissue
- spleen: 49 nTPM
- lymph node: 44 nTPM
- prostate: 31 nTPM
- small intestine: 28 nTPM
- skin: 24 nTPM
- appendix: 24 nTPM
Single-cell type
- b-cells: 125 nCPM
- paneth cells: 74 nCPM
- rod photoreceptor cells: 56 nCPM
- goblet cells: 49 nCPM
- prostatic glandular cells: 49 nCPM
- colonocytes: 49 nCPM
Immune cell
- naive B-cell: 15 nTPM
- memory B-cell: 12 nTPM
- NK-cell: 5.5 nTPM
- myeloid DC: 3.7 nTPM
- gdT-cell: 3.5 nTPM
- non-classical monocyte: 3.3 nTPM
Brain region
- choroid plexus: 19 nTPM
- medulla oblongata: 19 nTPM
- basal ganglia: 15 nTPM
- pons: 15 nTPM
- midbrain: 14 nTPM
- cerebral cortex: 14 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)
- 0.57
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.43
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RABEP2 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 RABEP2 as an antibody target. Whether an autoantibody or antibody against RABEP2 could matter depends on whether native RABEP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RABEP2 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 RABEP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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