LSAMP
Limbic system-associated membrane protein
Also known as: IGLON3, LAMP, LSAMP_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q13449
- Gene
- LSAMP
- Ensembl
- ENSG00000185565
- Chromosome
- 3
- Canonical length
- 338 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene encodes a member of the immunoglobulin LAMP, OBCAM and neurotrimin (IgLON) family of proteins. The encoded preproprotein is proteolytically processed to generate a neuronal surface glycoprotein. This protein may act as a selective homophilic adhesion molecule during axon guidance and neuronal growth in the developing limbic system. The encoded protein may also function as a tumor suppressor and may play a role in neuropsychiatric disorders. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed. [provided by RefSeq, Jan 2016]
Canonical amino-acid sequenceUniProt
338 residues, UniProt reviewed canonical sequence.
>Q13449|LSAMP
1 MVRRVQPDRK QLPLVLLRLL CLLPTGLPVR SVDFNRGTDN ITVRQGDTAI LRCVVEDKNS
61 KVAWLNRSGI IFAGHDKWSL DPRVELEKRH SLEYSLRIQK VDVYDEGSYT CSVQTQHEPK
121 TSQVYLIVQV PPKISNISSD VTVNEGSNVT LVCMANGRPE PVITWRHLTP TGREFEGEEE
181 YLEILGITRE QSGKYECKAA NEVSSADVKQ VKVTVNYPPT ITESKSNEAT TGRQASLKCE
241 ASAVPAPDFE WYRDDTRINS ANGLEIKSTE GQSSLTVTNV TEEHYGNYTC VAANKLGVTN
301 ASLVLFRPGS VRGINGSISL AVPLWLLAAS LLCLLSKCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LSAMP 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)
- 0.37
- Highest tissue expression
- 57 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 57 nTPM
- retina: 38 nTPM
- basal ganglia: 36 nTPM
- amygdala: 34 nTPM
- hypothalamus: 29 nTPM
- hippocampal formation: 28 nTPM
Single-cell type
- astrocytes: 8,317 nCPM
- bergmann glia: 6,745 nCPM
- oligodendrocyte progenitor cells: 5,356 nCPM
- retinal horizontal cells: 4,373 nCPM
- brain inhibitory neurons: 3,777 nCPM
- brain excitatory neurons: 3,274 nCPM
Immune cell
- basophil: 0.9 nTPM
- naive B-cell: 0.3 nTPM
- neutrophil: 0.3 nTPM
- naive CD4 T-cell: 0.2 nTPM
- eosinophil: 0.1 nTPM
- gdT-cell: 0.1 nTPM
Brain region
- cerebral cortex: 280 nTPM
- hippocampal formation: 265 nTPM
- thalamus: 251 nTPM
- amygdala: 228 nTPM
- basal ganglia: 222 nTPM
- hypothalamus: 210 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)
- 0.27
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 1.57
- DepMap mean gene effect
- 0.12
- 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
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads LSAMP as an antibody target. Whether an autoantibody or antibody against LSAMP could matter depends on whether native LSAMP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LSAMP is annotated at the cell surface, where native LSAMP 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 LSAMP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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