LAX1
Lymphocyte transmembrane adapter 1
Also known as: FLJ20340, LAX, LAX1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IWV1
- Gene
- LAX1
- Ensembl
- ENSG00000122188
- Chromosome
- 1
- Canonical length
- 398 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Golgi apparatus,Plasma membrane,Cytosol
OverviewNCBI Gene
Enables SH2 domain binding activity and protein kinase binding activity. Involved in several processes, including B cell activation; negative regulation of MAPK cascade; and negative regulation of T cell activation. Located in Golgi apparatus; cytosol; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
398 residues, UniProt reviewed canonical sequence.
>Q8IWV1|LAX1
1 MDGVTPTLST IRGRTLESST LHVTPRSLDR NKDQITNIFS GFAGLLAILL VVAVFCILWN
61 WNKRKKRQVP YLRVTVMPLL TLPQTRQRAK NIYDILPWRQ EDLGRHESRS MRIFSTESLL
121 SRNSESPEHV PSQAGNAFQE HTAHIHATEY AVGIYDNAMV PQMCGNLTPS AHCINVRASR
181 DCASISSEDS HDYVNVPTAE EIAETLASTK SPSRNLFVLP STQKLEFTEE RDEGCGDAGD
241 CTSLYSPGAE DSDSLSNGEG SSQISNDYVN MTGLDLSAIQ ERQLWVAFQC CRDYENVPAA
301 DPSGSQQQAE KDVPSSNIGH VEDKTDDPGT HVQCVKRTFL ASGDYADFQP FTQSEDSQMK
361 HREEMSNEDS SDYENVLTAK LGGRDSEQGP GTQLLPDELocalizationUniProt · AlphaFold · HPA
Whether an antibody against LAX1 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
- 1
- Mean surface accessibility (rSASA)
- 0.71
- Highest tissue expression
- 20 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 20 nTPM
- lymph node: 11 nTPM
- thymus: 10 nTPM
- appendix: 8.3 nTPM
- spleen: 6.8 nTPM
- urinary bladder: 4.8 nTPM
Single-cell type
- mast cells: 227 nCPM
- plasma cells: 103 nCPM
- t-cells: 61 nCPM
- nk-cells: 51 nCPM
- b-cells: 21 nCPM
- paneth cells: 16 nCPM
Immune cell
- gdT-cell: 12 nTPM
- memory CD8 T-cell: 9.4 nTPM
- MAIT T-cell: 9.1 nTPM
- T-reg: 8.1 nTPM
- memory B-cell: 7.5 nTPM
- memory CD4 T-cell: 7.1 nTPM
Brain region
- white matter: 2.6 nTPM
- pons: 2.4 nTPM
- medulla oblongata: 2.2 nTPM
- cerebellum: 2.1 nTPM
- cerebral cortex: 1.9 nTPM
- choroid plexus: 1.9 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)
- 1.17
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.43
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adaptive immune response
- antigen receptor-mediated signaling pathway
- B cell activation
- immune response
- intracellular signal transduction
- lymphocyte activation
- negative regulation of MAPK cascade
- negative regulation of T cell activation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Lymphocyte transmembrane adapter 1
- Lymphocyte activation family X
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LAX1 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 LAX1 as an antibody target. Whether an autoantibody or antibody against LAX1 could matter depends on whether native LAX1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LAX1 is annotated at the cell surface, where native LAX1 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 LAX1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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