PALM
Paralemmin-1
Also known as: KIAA0270, PALM_HUMAN, PALM1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75781
- Gene
- PALM
- Ensembl
- ENSG00000099864
- Chromosome
- 19
- Canonical length
- 387 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane
OverviewNCBI Gene
This gene encodes a member of the paralemmin protein family. The product of this gene is a prenylated and palmitoylated phosphoprotein that associates with the cytoplasmic face of plasma membranes and is implicated in plasma membrane dynamics in neurons and other cell types. Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
387 residues, UniProt reviewed canonical sequence.
>O75781|PALM
1 MEVLAAETTS QQERLQAIAE KRKRQAEIEN KRRQLEDERR QLQHLKSKAL RERWLLEGTP
61 SSASEGDEDL RRQMQDDEQK TRLLEDSVSR LEKEIEVLER GDSAPATAKE NAAAPSPVRA
121 PAPSPAKEER KTEVVMNSQQ TPVGTPKDKR VSNTPLRTVD GSPMMKAAMY SVEITVEKDK
181 VTGETRVLSS TTLLPRQPLP LGIKVYEDET KVVHAVDGTA ENGIHPLSSS EVDELIHKAD
241 EVTLSEAGST AGAAETRGAV EGAARTTPSR REITGVQAQP GEATSGPPGI QPGQEPPVTM
301 IFMGYQNVED EAETKKVLGL QDTITAELVV IEDAAEPKEP APPNGSAAEP PTEAASREEN
361 QAGPEATTSD PQDLDMKKHR CKCCSIMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PALM 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)
- 0.53
- Highest tissue expression
- 293 nTPM
Expression across tissuesHPA
Tissue
- amygdala: 293 nTPM
- cerebral cortex: 287 nTPM
- hippocampal formation: 245 nTPM
- basal ganglia: 222 nTPM
- hypothalamus: 107 nTPM
- midbrain: 107 nTPM
Single-cell type
- astrocytes: 125 nCPM
- lymphatic endothelial cells: 108 nCPM
- müller glia: 98 nCPM
- ependymal cells: 83 nCPM
- fibro-adipogenic progenitors: 81 nCPM
- leydig cells: 70 nCPM
Immune cell
- non-classical monocyte: 1.9 nTPM
- intermediate monocyte: 0.4 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- hippocampal formation: 271 nTPM
- cerebral cortex: 262 nTPM
- amygdala: 255 nTPM
- basal ganglia: 218 nTPM
- thalamus: 163 nTPM
- medulla oblongata: 151 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)
- 0.52
- gnomAD pLI
- 0.52
- gnomAD missense Z
- 0.72
- DepMap mean gene effect
- -0.07
- 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
- adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway
- cellular response to electrical stimulus
- cytoskeleton organization
- negative regulation of dopamine receptor signaling pathway
- positive regulation of filopodium assembly
- protein localization to plasma membrane
- regulation of cell shape
- synapse maturation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PALM 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 PALM as an antibody target. Whether an autoantibody or antibody against PALM could matter depends on whether native PALM is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PALM is annotated at the cell surface, where native PALM 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 PALM as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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