ITPRIP
Inositol 1,4,5-trisphosphate receptor-interacting protein
Also known as: bA127L20.2, DANGER, IPRI_HUMAN, KIAA1754
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IWB1
- Gene
- ITPRIP
- Ensembl
- ENSG00000148841
- Chromosome
- 10
- Canonical length
- 547 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
This gene encodes a membrane-associated protein that binds the inositol 1,4,5-trisphosphate receptor (ITPR). The encoded protein enhances the sensitivity of ITPR to intracellular calcium signaling. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]
Canonical amino-acid sequenceUniProt
547 residues, UniProt reviewed canonical sequence.
>Q8IWB1|ITPRIP
1 MAMGLFRVCL VVVTAIINHP LLFPRENATV PENEEEIIRK MQAHQEKLQL EQLRLEEEVA
61 RLAAEKEALE QVAEEGRQQN ETRVAWDLWS TLCMILFLMI EVWRQDHQEG PSPECLGGEE
121 DELPGLGGAP LQGLTLPNKA TLGHFYERCI RGATADAART REFLEGFVDD LLEALRSLCN
181 RDTDMEVEDF IGVDSMYENW QVDRPLLCHL FVPFTPPEPY RFHPELWCSG RSVPLDRQGY
241 GQIKVVRADG DTLSCICGKT KLGEDMLCLL HGRNSMAPPC GDMENLLCAT DSLYLDTMQV
301 MKWFQTALTR AWKGIAHKYE FDLAFGQLDS PGSLKIKFRS GKFMPFNLIP VIQCDDSDLY
361 FVSHLPREPS EGTPASSTDW LLSFAVYERH FLRTTLKALP EGACHLSCLQ IASFLLSKQS
421 RLTGPSGLSS YHLKTALLHL LLLRQAADWK AGQLDARLHE LLCFLEKSLL QKKLHHFFIG
481 NRKVPEAMGL PEAVLRAEPL NLFRPFVLQR SLYRKTLDSF YEMLKNAPAL ISEYSLHVPS
541 DQPTPKSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ITPRIP 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
- 1
- Mean surface accessibility (rSASA)
- 0.36
- Highest tissue expression
- 192 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 192 nTPM
- heart muscle: 69 nTPM
- skin: 63 nTPM
- esophagus: 50 nTPM
- vagina: 42 nTPM
- blood vessel: 41 nTPM
Single-cell type
- neutrophils: 802 nCPM
- esophageal apical cells: 239 nCPM
- esophageal suprabasal cells: 237 nCPM
- esophageal basal cells: 208 nCPM
- neutrophil progenitors: 170 nCPM
- suprabasal keratinocytes: 144 nCPM
Immune cell
- neutrophil: 31 nTPM
- total PBMC: 21 nTPM
- eosinophil: 14 nTPM
- classical monocyte: 9.5 nTPM
- myeloid DC: 6.3 nTPM
- non-classical monocyte: 5.9 nTPM
Brain region
- choroid plexus: 27 nTPM
- cerebral cortex: 18 nTPM
- medulla oblongata: 12 nTPM
- thalamus: 12 nTPM
- white matter: 11 nTPM
- spinal cord: 10 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)
- 1.5
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.56
- DepMap mean gene effect
- -0.01
- 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
- extrinsic apoptotic signaling pathway via death domain receptors
- negative regulation of extrinsic apoptotic signaling pathway via death domain receptors
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ITPRIP in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
- ITPR
- PGRMC2
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ITPRIP as an antibody target. Whether an autoantibody or antibody against ITPRIP could matter depends on whether native ITPRIP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ITPRIP is annotated at the cell surface, where native ITPRIP 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 ITPRIP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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