ARL6IP5
PRA1 family protein 3
Also known as: DERP11, GTRAP3-18, HSPC127, JWA, PRAF3, PRAF3_HUMAN, Yip6b
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75915
- Gene
- ARL6IP5
- Ensembl
- ENSG00000144746
- Chromosome
- 3
- Canonical length
- 188 aa
- Protein class
- Predicted membrane proteins, Transporters
- Subcellular location
- Endoplasmic reticulum
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Expression of this gene is affected by vitamin A. The encoded protein of this gene may be associated with the cytoskeleton. A similar protein in rats may play a role in the regulation of cell differentiation. The rat protein binds and inhibits the cell membrane glutamate transporter EAAC1. The expression of the rat gene is upregulated by retinoic acid, which results in a specific reduction in EAAC1-mediated glutamate transport. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
188 residues, UniProt reviewed canonical sequence.
>O75915|ARL6IP5
1 MDVNIAPLRA WDDFFPGSDR FARPDFRDIS KWNNRVVSNL LYYQTNYLVV AAMMISIVGF
61 LSPFNMILGG IVVVLVFTGF VWAAHNKDVL RRMKKRYPTT FVMVVMLASY FLISMFGGVM
121 VFVFGITFPL LLMFIHASLR LRNLKNKLEN KMEGIGLKRT PMGIVLDALE QQEEGINRLT
181 DYISKVKELocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARL6IP5 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
- 2
- Mean surface accessibility (rSASA)
- 0.38
- Highest tissue expression
- 203 nTPM
Expression across tissuesHPA
Tissue
- heart muscle: 203 nTPM
- tongue: 174 nTPM
- skeletal muscle: 172 nTPM
- blood vessel: 163 nTPM
- salivary gland: 151 nTPM
- adipose tissue: 148 nTPM
Single-cell type
- platelets: 1,165 nCPM
- salivary ionocytes: 565 nCPM
- extravillous trophoblasts: 523 nCPM
- breast lactating cells: 481 nCPM
- cytotrophoblasts: 370 nCPM
- neutrophils: 349 nCPM
Immune cell
- total PBMC: 932 nTPM
- basophil: 698 nTPM
- eosinophil: 651 nTPM
- T-reg: 532 nTPM
- memory CD4 T-cell: 464 nTPM
- memory CD8 T-cell: 427 nTPM
Brain region
- white matter: 119 nTPM
- pons: 104 nTPM
- hypothalamus: 103 nTPM
- spinal cord: 100 nTPM
- cerebellum: 92 nTPM
- medulla oblongata: 89 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)
- 1.25
- gnomAD pLI
- 0.1
- gnomAD missense Z
- 0.37
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- selective
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
- cellular response to oxidative stress
- glutathione metabolic process
- intrinsic apoptotic signaling pathway in response to oxidative stress
- L-glutamate import across plasma membrane
- L-glutamate transmembrane transport
- learning or memory
- negative regulation of L-glutamate import across plasma membrane
- negative regulation of mitochondrial membrane potential
- negative regulation of transport
- positive regulation of apoptotic process
- positive regulation of stress-activated MAPK cascade
- protein localization to plasma membrane
- protein transport
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ARL6IP5 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 ARL6IP5 as an antibody target. Whether an autoantibody or antibody against ARL6IP5 could matter depends on whether native ARL6IP5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARL6IP5 is annotated at the cell surface, where native ARL6IP5 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 ARL6IP5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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