RILPL2
RILP-like protein 2
Also known as: FLJ30380, FLJ32372, MGC7036, RIPL2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q969X0
- Gene
- RILPL2
- Ensembl
- ENSG00000150977
- Chromosome
- 12
- Canonical length
- 211 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles,Primary cilium,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a protein that contains a rab-interacting lysosomal protein-like domain. This protein may be involved in regulating lysosome morphology. This protein may also be a target for the Hepatitis C virus and assist in viral replication. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]
Canonical amino-acid sequenceUniProt
211 residues, UniProt reviewed canonical sequence.
>Q969X0|RILPL2
1 MEEPPVREEE EEEGEEDEER DEVGPEGALG KSPFQLTAED VYDISYLLGR ELMALGSDPR
61 VTQLQFKVVR VLEMLEALVN EGSLALEELK MERDHLRKEV EGLRRQSPPA SGEVNLGPNK
121 MVVDLTDPNR PRFTLQELRD VLQERNKLKS QLLVVQEELQ CYKSGLIPPR EGPGGRREKD
181 AVVTSAKNAG RNKEEKTIIK KLFFFRSGKQ TLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RILPL2 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
- 110 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 110 nTPM
- blood vessel: 47 nTPM
- spleen: 35 nTPM
- choroid plexus: 34 nTPM
- lung: 33 nTPM
- thyroid gland: 28 nTPM
Single-cell type
- neutrophils: 3,538 nCPM
- monocytes: 792 nCPM
- monocyte progenitors: 473 nCPM
- neutrophil progenitors: 456 nCPM
- megakaryocytes: 433 nCPM
- cdc: 391 nCPM
Immune cell
- neutrophil: 177 nTPM
- eosinophil: 160 nTPM
- classical monocyte: 133 nTPM
- non-classical monocyte: 122 nTPM
- intermediate monocyte: 106 nTPM
- basophil: 99 nTPM
Brain region
- choroid plexus: 18 nTPM
- hypothalamus: 11 nTPM
- cerebral cortex: 10 nTPM
- medulla oblongata: 9.3 nTPM
- midbrain: 9.3 nTPM
- thalamus: 9.2 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)
- 1.15
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.52
- DepMap mean gene effect
- -0.16
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cilium assembly
- epithelial cell morphogenesis
- protein transport from ciliary membrane to plasma membrane
Molecular functions
- dynein light intermediate chain binding
- identical protein binding
- protein dimerization activity
- small GTPase binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RILPL2 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 RILPL2 as an antibody target. Whether an autoantibody or antibody against RILPL2 could matter depends on whether native RILPL2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RILPL2 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 RILPL2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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