LYPD1
Ly6/PLAUR domain-containing protein 1
Also known as: LYPD1_HUMAN, LYPDC1, MGC29643
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N2G4
- Gene
- LYPD1
- Ensembl
- ENSG00000150551
- Chromosome
- 2
- Canonical length
- 141 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles,Plasma membrane
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
Predicted to enable acetylcholine receptor inhibitor activity. Predicted to be involved in acetylcholine receptor signaling pathway. Predicted to act upstream of or within several processes, including behavioral fear response; cholinergic synaptic transmission; and negative regulation of protein localization to plasma membrane. Predicted to be located in extracellular region and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
141 residues, UniProt reviewed canonical sequence.
>Q8N2G4|LYPD1
1 MWVLGIAATF CGLFLLPGFA LQIQCYQCEE FQLNNDCSSP EFIVNCTVNV QDMCQKEVME
61 QSAGIMYRKS CASSAACLIA SAGYQSFCSP GKLNSVCISC CNTPLCNGPR PKKRGSSASA
121 LRPGLRTTIL FLKLALFSAH CLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LYPD1 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
- 0
- Mean surface accessibility (rSASA)
- 0.44
- Highest tissue expression
- 50 nTPM
Expression across tissuesHPA
Tissue
- fallopian tube: 50 nTPM
- basal ganglia: 36 nTPM
- midbrain: 25 nTPM
- hypothalamus: 23 nTPM
- hippocampal formation: 22 nTPM
- amygdala: 20 nTPM
Single-cell type
- fallopian secretory cells: 249 nCPM
- oocytes: 175 nCPM
- pituitary stem cells: 129 nCPM
- oligodendrocyte progenitor cells: 57 nCPM
- ependymal cells: 52 nCPM
- epididymal efferent duct ciliated cells: 47 nCPM
Immune cell
- eosinophil: 3.6 nTPM
- basophil: 0.6 nTPM
- naive B-cell: 0.1 nTPM
- classical monocyte: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- hypothalamus: 39 nTPM
- medulla oblongata: 38 nTPM
- midbrain: 37 nTPM
- thalamus: 34 nTPM
- pons: 32 nTPM
- spinal cord: 31 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)
- 1.74
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.5
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- acetylcholine receptor signaling pathway
- behavioral fear response
- negative regulation of protein localization to plasma membrane
- protein localization to plasma membrane
- response to nicotine
- synaptic transmission, cholinergic
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LYPD1 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 LYPD1 as an antibody target. Whether an autoantibody or antibody against LYPD1 could matter depends on whether native LYPD1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LYPD1 is annotated at the cell surface, where native LYPD1 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 LYPD1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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