RABEPK
Rab9 effector protein with kelch motifs
Also known as: bA65N13.1, RAB9P40, RABEK_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7Z6M1
- Gene
- RABEPK
- Ensembl
- ENSG00000136933
- Chromosome
- 9
- Canonical length
- 372 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
Predicted to be involved in receptor-mediated endocytosis and vesicle docking involved in exocytosis. Located in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
372 residues, UniProt reviewed canonical sequence.
>Q7Z6M1|RABEPK
1 MKQLPVLEPG DKPRKATWYT LTVPGDSPCA RVGHSCSYLP PVGNAKRGKV FIVGGANPNR
61 SFSDVHTMDL GKHQWDLDTC KGLLPRYEHA SFIPSCTPDR IWVFGGANQS GNRNCLQVLN
121 PETRTWTTPE VTSPPPSPRT FHTSSAAIGN QLYVFGGGER GAQPVQDTKL HVFDANTLTW
181 SQPETLGNPP SPRHGHVMVA AGTKLFIHGG LAGDRFYDDL HCIDISDMKW QKLNPTGAAP
241 AGCAAHSAVA MGKHVYIFGG MTPAGALDTM YQYHTEEQHW TLLKFDTLLP PGRLDHSMCI
301 IPWPVTCASE KEDSNSLTLN HEAEKEDSAD KVMSHSGDSH EESQTATLLC LVFGGMNTEG
361 EIYDDCIVTV VDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RABEPK 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 55 nTPM
Expression across tissuesHPA
Tissue
- liver: 55 nTPM
- basal ganglia: 29 nTPM
- cerebral cortex: 24 nTPM
- midbrain: 23 nTPM
- hypothalamus: 21 nTPM
- amygdala: 20 nTPM
Single-cell type
- hepatocytes: 110 nCPM
- late primary spermatocytes: 86 nCPM
- early spermatids: 78 nCPM
- cytotrophoblasts: 63 nCPM
- migrating cytotrophoblasts: 59 nCPM
- hepatic stellate cells: 58 nCPM
Immune cell
- T-reg: 39 nTPM
- naive CD4 T-cell: 38 nTPM
- memory CD4 T-cell: 35 nTPM
- naive CD8 T-cell: 28 nTPM
- neutrophil: 28 nTPM
- basophil: 28 nTPM
Brain region
- thalamus: 29 nTPM
- basal ganglia: 28 nTPM
- hypothalamus: 27 nTPM
- white matter: 26 nTPM
- midbrain: 26 nTPM
- pons: 26 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)
- 1.39
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.05
- DepMap mean gene effect
- -0.12
- DepMap dependency class
- selective
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
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Kelch-type beta-propeller
- KLHDC2/KLHL20/DRC7 Kelch-repeats domain
- Rab9 effector with kelch motifs
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RABEPK in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
- PIKFYVE
- RAB9
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads RABEPK as an antibody target. Whether an autoantibody or antibody against RABEPK could matter depends on whether native RABEPK is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RABEPK 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 RABEPK as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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