STAMBPL1
AMSH-like protease
Also known as: ALMalpha, AMSH-FP, AMSH-LP, bA399O19.2, FLJ31524, KIAA1373, STALP_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96FJ0
- Gene
- STAMBPL1
- Ensembl
- ENSG00000138134
- Chromosome
- 10
- Canonical length
- 436 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Plasma membrane
OverviewNCBI Gene
Enables K63-linked deubiquitinase activity. Involved in cellular response to L-leucine and positive regulation of TORC1 signaling. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
436 residues, UniProt reviewed canonical sequence.
>Q96FJ0|STAMBPL1
1 MDQPFTVNSL KKLAAMPDHT DVSLSPEERV RALSKLGCNI TISEDITPRR YFRSGVEMER
61 MASVYLEEGN LENAFVLYNK FITLFVEKLP NHRDYQQCAV PEKQDIMKKL KEIAFPRTDE
121 LKNDLLKKYN VEYQEYLQSK NKYKAEILKK LEHQRLIEAE RKRIAQMRQQ QLESEQFLFF
181 EDQLKKQELA RGQMRSQQTS GLSEQIDGSA LSCFSTHQNN SLLNVFADQP NKSDATNYAS
241 HSPPVNRALT PAATLSAVQN LVVEGLRCVV LPEDLCHKFL QLAESNTVRG IETCGILCGK
301 LTHNEFTITH VIVPKQSAGP DYCDMENVEE LFNVQDQHDL LTLGWIHTHP TQTAFLSSVD
361 LHTHCSYQLM LPEAIAIVCS PKHKDTGIFR LTNAGMLEVS ACKKKGFHPH TKEPRLFSIC
421 KHVLVKDIKI IVLDLRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against STAMBPL1 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)
- 0.35
- Highest tissue expression
- 23 nTPM
Expression across tissuesHPA
Tissue
- adrenal gland: 23 nTPM
- testis: 17 nTPM
- lymph node: 15 nTPM
- tonsil: 12 nTPM
- cerebral cortex: 11 nTPM
- ovary: 9.8 nTPM
Single-cell type
- vascular smooth muscle cells: 338 nCPM
- microglia: 149 nCPM
- adrenal cortex cells: 135 nCPM
- pericytes: 95 nCPM
- late primary spermatocytes: 89 nCPM
- ependymal cells: 78 nCPM
Immune cell
- T-reg: 28 nTPM
- plasmacytoid DC: 28 nTPM
- NK-cell: 24 nTPM
- memory B-cell: 18 nTPM
- naive CD4 T-cell: 17 nTPM
- memory CD4 T-cell: 16 nTPM
Brain region
- cerebral cortex: 31 nTPM
- basal ganglia: 24 nTPM
- white matter: 24 nTPM
- pons: 19 nTPM
- cerebellum: 18 nTPM
- spinal cord: 17 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)
- 1.27
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.27
- DepMap mean gene effect
- 0.02
- 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 response to L-leucine
- positive regulation of TORC1 signaling
- protein deubiquitination
- protein K63-linked deubiquitination
- proteolysis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of STAMBPL1 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 STAMBPL1 as an antibody target. Whether an autoantibody or antibody against STAMBPL1 could matter depends on whether native STAMBPL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
STAMBPL1 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 STAMBPL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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