RAB11FIP2
Rab11 family-interacting protein 2
Also known as: KIAA0941, nRip11, Rab11-FIP2, RFIP2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7L804
- Gene
- RAB11FIP2
- Ensembl
- ENSG00000107560
- Chromosome
- 10
- Canonical length
- 512 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles
- Quaternary structure
- Homooligomer
OverviewNCBI Gene
Enables protein homodimerization activity and protein kinase binding activity. Involved in several processes, including TRAM-dependent toll-like receptor 4 signaling pathway; phagocytosis; and positive regulation of GTPase activity. Located in endosome; nucleoplasm; and phagocytic cup. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
512 residues, UniProt reviewed canonical sequence.
>Q7L804|RAB11FIP2
1 MMLSEQAQKW FPTHVQVTVL QAKDLKPKGK SGTNDTYTII QLGKEKYSTS VAEKTLEPVW
61 KEEASFELPG LLIQGSPEKY ILFLIVMHRS LVGLDKFLGQ VAINLNDIFE DKQRRKTEWF
121 RLESKQGKRI KNRGEIKVNI QFMRNNMTAS MFDLSMKDKT RSPFAKLKDK MKGRKNDGTF
181 SDTSSAIIPS THMPDANSEF SSGEIQMKSK PKKPFLLGPQ RLSSAHSMSD LSGSHMSSEK
241 LKAGTIGQTH LLGHQLDSFG TVPESGSLKS PHRRTLSFDT SKMNQPDSIV DEGELCFGRQ
301 NDPFTNVTAS LPQKFATLPR KKNPFEESSE TWDSSMNLFS KPIEIRKENK REKREKVSLF
361 ERVTGKKDSR RSDKLNNGGS DSPCDLKSPN AFSENRQDYF DYESTNPFTA KFRASNIMPS
421 SSFHMSPTSN EDLRKIPDSN PFDATAGYRS LTYEEVLQEL VKHKELLRRK DTHIRELEDY
481 IDNLLVRVME ETPSILRVPY EPSRKAGKFS NSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RAB11FIP2 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.58
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 27 nTPM
- seminal vesicle: 23 nTPM
- smooth muscle: 18 nTPM
- endometrium: 18 nTPM
- stomach: 16 nTPM
- bone marrow: 13 nTPM
Single-cell type
- parietal cells: 327 nCPM
- epididymal efferent duct absorptive cells: 229 nCPM
- renal collecting duct principal cells: 201 nCPM
- neutrophil progenitors: 182 nCPM
- renal connecting tubule cells: 169 nCPM
- epididymal basal cells: 149 nCPM
Immune cell
- plasmacytoid DC: 0.5 nTPM
- naive B-cell: 0.4 nTPM
- naive CD4 T-cell: 0.4 nTPM
- memory B-cell: 0.3 nTPM
- neutrophil: 0.3 nTPM
- basophil: 0.2 nTPM
Brain region
- cerebral cortex: 25 nTPM
- basal ganglia: 24 nTPM
- hippocampal formation: 22 nTPM
- white matter: 21 nTPM
- thalamus: 20 nTPM
- amygdala: 20 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)
- 0.35
- gnomAD pLI
- 0.94
- gnomAD missense Z
- 0.78
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- establishment of cell polarity
- insulin secretion involved in cellular response to glucose stimulus
- phagocytosis
- positive regulation of GTPase activity
- positive regulation of protein localization to plasma membrane
- regulated exocytosis
- TRAM-dependent toll-like receptor 4 signaling pathway
Molecular functions
- identical protein binding
- protein homodimerization activity
- protein kinase binding
- small GTPase binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RAB11FIP2 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 RAB11FIP2 as an antibody target. Whether an autoantibody or antibody against RAB11FIP2 could matter depends on whether native RAB11FIP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RAB11FIP2 is annotated at the cell surface, where native RAB11FIP2 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label RAB11FIP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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