TIPRL
TIP41-like protein
Also known as: dJ69E11.3, MGC3794, TIP41, TIPRL_HUMAN, TIPRL1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75663
- Gene
- TIPRL
- Ensembl
- ENSG00000143155
- Chromosome
- 1
- Canonical length
- 272 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
TIPRL is an inhibitory regulator of protein phosphatase-2A (PP2A) (see PPP2CA; MIM 176915), PP4 (see PPP4C; MIM 602035), and PP6 (see PPP6C; MIM 612725) (McConnell et al., 2007 [PubMed 17384681]).[supplied by OMIM, Nov 2010]
Canonical amino-acid sequenceUniProt
272 residues, UniProt reviewed canonical sequence.
>O75663|TIPRL
1 MMIHGFQSSH RDFCFGPWKL TASKTHIMKS ADVEKLADEL HMPSLPEMMF GDNVLRIQHG
61 SGFGIEFNAT DALRCVNNYQ GMLKVACAEE WQESRTEGEH SKEVIKPYDW TYTTDYKGTL
121 LGESLKLKVV PTTDHIDTEK LKAREQIKFF EEVLLFEDEL HDHGVSSLSV KIRVMPSSFF
181 LLLRFFLRID GVLIRMNDTR LYHEADKTYM LREYTSRESK ISSLMHVPPS LFTEPNEISQ
241 YLPIKEAVCE KLIFPERIDP NPADSQKSTQ VELocalizationUniProt · AlphaFold · HPA
Whether an antibody against TIPRL 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)
- 0.33
- Highest tissue expression
- 32 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 32 nTPM
- thymus: 28 nTPM
- parathyroid gland: 26 nTPM
- skeletal muscle: 23 nTPM
- heart muscle: 22 nTPM
- endometrium: 22 nTPM
Single-cell type
- early primary spermatocytes: 155 nCPM
- esophageal apical cells: 145 nCPM
- late primary spermatocytes: 143 nCPM
- esophageal suprabasal cells: 117 nCPM
- esophageal basal cells: 100 nCPM
- hofbauer cells: 85 nCPM
Immune cell
- basophil: 71 nTPM
- eosinophil: 37 nTPM
- T-reg: 36 nTPM
- neutrophil: 35 nTPM
- non-classical monocyte: 34 nTPM
- intermediate monocyte: 32 nTPM
Brain region
- cerebral cortex: 34 nTPM
- hypothalamus: 29 nTPM
- basal ganglia: 28 nTPM
- hippocampal formation: 27 nTPM
- white matter: 25 nTPM
- cerebellum: 25 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)
- 0.34
- gnomAD pLI
- 0.95
- gnomAD missense Z
- 1.8
- DepMap mean gene effect
- -0.38
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 15% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- TIP41-like protein
- Phosphatase regulators and Met sulfoxide reductases
- TIP41-like family
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TIPRL 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 TIPRL as an antibody target. Whether an autoantibody or antibody against TIPRL could matter depends on whether native TIPRL is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TIPRL 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 TIPRL as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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