EXOC3L1
Exocyst complex component 3-like protein
Also known as: EX3L1_HUMAN, EXOC3L, FLJ35539, FLJ35587
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86VI1
- Gene
- EXOC3L1
- Ensembl
- ENSG00000179044
- Chromosome
- 16
- Canonical length
- 746 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles,Plasma membrane
OverviewNCBI Gene
Predicted to enable SNARE binding activity. Predicted to be involved in exocyst localization; exocytosis; and peptide hormone secretion. Predicted to be located in secretory granule. Predicted to be part of exocyst. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
746 residues, UniProt reviewed canonical sequence.
>Q86VI1|EXOC3L1
1 MDSAAKDEMQ PALSPGPEWP EQERAEQLAR GAALKWASGI FYRPEQLARL GQYRSREVQR
61 TCSLESRLKS VMQSYLEGVQ TGVWQLAQAI EVVQGTREAL SQARGLLQGM SQALQTLEPL
121 RERVAQHKQL QALSHLLPRL RAVPAAVSHT QTLIDGQQFL EAYVSLRELE QLREDTWAPL
181 GGLELPVFQG LDLLFEALGQ AVEAAAGAAG KLAREDPALL VAAVRVAEVE TGRTTPLGQV
241 PRDWRQRCLR ALQEGLEQAH FGSPLLPAPG ALPGWLEALR VALPVELATA EALVAPCCPP
301 QYNVVQLWAH TLHSGLRRSL QNLLAGPELE AADAFALLHW ALHVYLGQEM MGSLELGPEA
361 DVSQLEPLLT LENIEQLEAT FVANIQASVS QWLQNALDGE VAEWGREHGP NTDPSGSYYS
421 PMPAIVLQIL EENIRVASLV SESLQQRVHG MALSELGTFL RSFSDALIRF SRDHFRGKSM
481 APHYVPYLLA ALNHKSALSS SVSVLQLDGA PSGALAPVEA ALDELQRRIY RLVLEALQAE
541 LQPLFADLPS RQWLSSPELL QSVCERTGRF CRDFWRVRNP TVQLLLAEAE RAVVLQYLSA
601 LMQGRLVCRG ADERTQAAER LRHDAAQLQQ LFLSLGLEEN AHCAPVLLAL RELLNLRDPA
661 LLGLEVAGLR QQFPDVSEDH VSALLGLRGD LSREQHLAAL SSLQAALPPS PRASRRVLFS
721 LVPAPALAPA SCLPSGSCAR ALLLAELocalizationUniProt · AlphaFold · HPA
Whether an antibody against EXOC3L1 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)
- 0.32
- Highest tissue expression
- 44 nTPM
Expression across tissuesHPA
Tissue
- spleen: 44 nTPM
- lung: 9.6 nTPM
- kidney: 7.2 nTPM
- thyroid gland: 7 nTPM
- adipose tissue: 6.1 nTPM
- placenta: 5.5 nTPM
Single-cell type
- lymphatic endothelial cells: 28 nCPM
- ovarian stromal cells: 21 nCPM
- peritubular myoid cells: 20 nCPM
- vascular endothelial cells: 18 nCPM
- granulosa cells: 15 nCPM
- early primary spermatocytes: 12 nCPM
Immune cell
- non-classical monocyte: 0.4 nTPM
- neutrophil: 0.3 nTPM
- classical monocyte: 0.2 nTPM
- intermediate monocyte: 0.1 nTPM
- myeloid DC: 0.1 nTPM
- basophil: 0 nTPM
Brain region
- pons: 3.9 nTPM
- cerebellum: 3.7 nTPM
- cerebral cortex: 2.8 nTPM
- medulla oblongata: 2.8 nTPM
- amygdala: 2.7 nTPM
- hypothalamus: 2.7 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)
- 1.15
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.33
- DepMap mean gene effect
- -0.11
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of EXOC3L1 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 EXOC3L1 as an antibody target. Whether an autoantibody or antibody against EXOC3L1 could matter depends on whether native EXOC3L1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EXOC3L1 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 EXOC3L1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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