RAB3IP
Rab-3A-interacting protein
Also known as: FLJ22548, RAB3I_HUMAN, RABIN3, RABIN8
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96QF0
- Gene
- RAB3IP
- Ensembl
- ENSG00000127328
- Chromosome
- 12
- Canonical length
- 476 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Centrosome,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables guanyl-nucleotide exchange factor activity and identical protein binding activity. Involved in several processes, including positive regulation of cilium assembly; protein localization to motile cilium; and protein targeting to membrane. Located in centrosome; cytosol; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
476 residues, UniProt reviewed canonical sequence.
>Q96QF0|RAB3IP
1 MGLKKMKGLS YDEAFAMAND PLEGFHEVNL ASPTSPDLLG VYESGTQEQT TSPSVIYRPH
61 PSALSSVPIQ ANALDVSELP TQPVYSSPRR LNCAEISSIS FHVTDPAPCS TSGVTAGLTK
121 LTTRKDNYNA EREFLQGATI TEACDGSDDI FGLSTDSLSR LRSPSVLEVR EKGYERLKEE
181 LAKAQRELKL KDEECERLSK VRDQLGQELE ELTASLFEEA HKMVREANIK QATAEKQLKE
241 AQGKIDVLQA EVAALKTLVL SSSPTSPTQE PLPGGKTPFK KGHTRNKSTS SAMSGSHQDL
301 SVIQPIVKDC KEADLSLYNE FRLWKDEPTM DRTCPFLDKI YQEDIFPCLT FSKSELASAV
361 LEAVENNTLS IEPVGLQPIR FVKASAVECG GPKKCALTGQ SKSCKHRIKL GDSSNYYYIS
421 PFCRYRITSV CNFFTYIRYI QQGLVKQQDV DQMFWEVMQL RKEMSLAKLG YFKEELLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RAB3IP 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)
- 0.54
- Highest tissue expression
- 110 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 110 nTPM
- retina: 82 nTPM
- testis: 70 nTPM
- kidney: 45 nTPM
- epididymis: 42 nTPM
- cerebellum: 32 nTPM
Single-cell type
- late spermatids: 475 nCPM
- choroid plexus epithelial cells: 316 nCPM
- retinal pigment epithelial cells: 230 nCPM
- early spermatids: 219 nCPM
- epididymal clear cells: 182 nCPM
- endometrial glandular cells: 181 nCPM
Immune cell
- T-reg: 13 nTPM
- naive CD4 T-cell: 9.4 nTPM
- memory B-cell: 9.3 nTPM
- naive CD8 T-cell: 9.2 nTPM
- naive B-cell: 8.7 nTPM
- MAIT T-cell: 8.5 nTPM
Brain region
- cerebellum: 180 nTPM
- choroid plexus: 123 nTPM
- pons: 68 nTPM
- white matter: 65 nTPM
- medulla oblongata: 63 nTPM
- midbrain: 59 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)
- 0.89
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.67
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- none
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
- ciliary basal body-plasma membrane docking
- cilium assembly
- Golgi to plasma membrane transport
- negative regulation of filopodium assembly
- protein targeting to membrane
- protein transport
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RAB3IP 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 RAB3IP as an antibody target. Whether an autoantibody or antibody against RAB3IP could matter depends on whether native RAB3IP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RAB3IP 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 RAB3IP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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