LZTS3
Leucine zipper putative tumor suppressor 3
Also known as: KIAA0552, LZTS3_HUMAN, ProSAPiP1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O60299
- Gene
- LZTS3
- Ensembl
- ENSG00000088899
- Chromosome
- 20
- Canonical length
- 673 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles
- Quaternary structure
- Homooligomer
OverviewNCBI Gene
Predicted to enable PDZ domain binding activity. Predicted to be involved in protein homooligomerization; regulation of dendritic spine morphogenesis; and regulation of postsynapse assembly. Predicted to be located in postsynaptic density. Predicted to be active in dendritic spine and glutamatergic synapse. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
673 residues, UniProt reviewed canonical sequence.
>O60299|LZTS3
1 MAKLETLPVR ADPGRDPLLA FAPRPSELGP PDPRLAMGSV GSGVAHAQEF AMKSVGTRTG
61 GGGSQGSFPG PRGSGSGASR ERPGRYPSED KGLANSLYLN GELRGSDHTD VCGNVVGSSG
121 GSSSSGGSDK APPQYREPSH PPKLLATSGK LDQCSEPLVR PSAFKPVVPK NFHSMQNLCP
181 PQTNGTPEGR QGPGGLKGGL DKSRTMTPAG GSGSGLSDSG RNSLTSLPTY SSSYSQHLAP
241 LSASTSHINR IGTASYGSGS GGSSGGGSGY QDLGTSDSGR ASSKSGSSSS MGRPGHLGSG
301 EGGGGGLPFA ACSPPSPSAL IQELEERLWE KEQEVAALRR SLEQSEAAVA QVLEERQKAW
361 ERELAELRQG CSGKLQQVAR RAQRAQQGLQ LQVLRLQQDK KQLQEEAARL MRQREELEDK
421 VAACQKEQAD FLPRIEETKW EVCQKAGEIS LLKQQLKDSQ ADVSQKLSEI VGLRSQLREG
481 RASLREKEEQ LLSLRDSFSS KQASLELGEG ELPAACLKPA LTPVDPAEPQ DALATCESDE
541 AKMRRQAGVA AAASLVSVDG EAEAGGESGT RALRREVGRL QAELAAERRA RERQGASFAE
601 ERRVWLEEKE KVIEYQKQLQ LSYVEMYQRN QQLERRLRER GAAGGASTPT PQHGEEKKAW
661 TPSRLERIES TEILocalizationUniProt · AlphaFold · HPA
Whether an antibody against LZTS3 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)
- 0.62
- Highest tissue expression
- 175 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 175 nTPM
- cerebral cortex: 114 nTPM
- basal ganglia: 94 nTPM
- amygdala: 57 nTPM
- hippocampal formation: 56 nTPM
- retina: 50 nTPM
Single-cell type
- rod photoreceptor cells: 64 nCPM
- lacrimal acinar cells: 63 nCPM
- brain excitatory neurons: 61 nCPM
- brain inhibitory neurons: 52 nCPM
- salivary ionocytes: 52 nCPM
- salivary acinar cells: 41 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- basal ganglia: 186 nTPM
- cerebral cortex: 180 nTPM
- hippocampal formation: 159 nTPM
- amygdala: 139 nTPM
- cerebellum: 139 nTPM
- white matter: 132 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)
- 0.23
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.75
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LZTS3 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 LZTS3 as an antibody target. Whether an autoantibody or antibody against LZTS3 could matter depends on whether native LZTS3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LZTS3 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 LZTS3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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