LYPLAL1
Lysophospholipase-like protein 1
Also known as: LYPL1_HUMAN, Q96AV0
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5VWZ2
- Gene
- LYPLAL1
- Ensembl
- ENSG00000143353
- Chromosome
- 1
- Canonical length
- 237 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Enables palmitoyl-(protein) hydrolase activity. Involved in negative regulation of cGAS/STING signaling pathway. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
237 residues, UniProt reviewed canonical sequence.
>Q5VWZ2|LYPLAL1
1 MAAASGSVLQ RCIVSPAGRH SASLIFLHGS GDSGQGLRMW IKQVLNQDLT FQHIKIIYPT
61 APPRSYTPMK GGISNVWFDR FKITNDCPEH LESIDVMCQV LTDLIDEEVK SGIKKNRILI
121 GGFSMGGCMA IHLAYRNHQD VAGVFALSSF LNKASAVYQA LQKSNGVLPE LFQCHGTADE
181 LVLHSWAEET NSMLKSLGVT TKFHSFPNVY HELSKTELDI LKLWILTKLP GEMEKQKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LYPLAL1 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)
- 0.25
- Highest tissue expression
- 40 nTPM
Expression across tissuesHPA
Tissue
- kidney: 40 nTPM
- heart muscle: 34 nTPM
- liver: 26 nTPM
- adrenal gland: 17 nTPM
- spinal cord: 16 nTPM
- thyroid gland: 15 nTPM
Single-cell type
- choroid plexus epithelial cells: 476 nCPM
- myonuclei: 258 nCPM
- platelets: 248 nCPM
- adrenal cortex cells: 242 nCPM
- retinal pigment epithelial cells: 239 nCPM
- distal convoluted tubule cells: 206 nCPM
Immune cell
- memory B-cell: 3.3 nTPM
- naive CD4 T-cell: 2.3 nTPM
- neutrophil: 2.2 nTPM
- classical monocyte: 2 nTPM
- naive B-cell: 2 nTPM
- MAIT T-cell: 1.9 nTPM
Brain region
- white matter: 7.2 nTPM
- hypothalamus: 6.5 nTPM
- spinal cord: 5.4 nTPM
- medulla oblongata: 5.2 nTPM
- cerebellum: 5 nTPM
- basal ganglia: 4.5 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)
- 1.4
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.23
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of cGAS/STING signaling pathway
- negative regulation of Golgi to plasma membrane protein transport
Molecular functions
- hydrolase activity, acting on ester bonds
- palmitoyl-(protein) hydrolase activity
- phosphatidylcholine lysophospholipase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads LYPLAL1 as an antibody target. Whether an autoantibody or antibody against LYPLAL1 could matter depends on whether native LYPLAL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LYPLAL1 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 LYPLAL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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