SYCE3
Synaptonemal complex central element protein 3
Also known as: C22orf41, SYCE3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A1L190
- Gene
- SYCE3
- Ensembl
- ENSG00000217442
- Chromosome
- 22
- Canonical length
- 88 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Golgi apparatus
- Quaternary structure
- Homotetramer
OverviewNCBI Gene
Predicted to be involved in reciprocal meiotic recombination; spermatogenesis; and synaptonemal complex assembly. Predicted to act upstream of or within positive regulation of apoptotic process; positive regulation of developmental process; and positive regulation of reproductive process. Predicted to be located in chromosome and nucleus. Predicted to be active in central element. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
88 residues, UniProt reviewed canonical sequence.
>A1L190|SYCE3
1 MDDADPEERN YDNMLKMLSD LNKDLEKLLE EMEKISVQAT WMAYDMVVMR TNPTLAESMR
61 RLEDAFVNCK EEMEKNWQEL LHETKQRLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SYCE3 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)
- 0.5
- Highest tissue expression
- 133 nTPM
Expression across tissuesHPA
Tissue
- testis: 133 nTPM
- kidney: 2.5 nTPM
- midbrain: 2.4 nTPM
- basal ganglia: 2.3 nTPM
- amygdala: 2 nTPM
- cerebral cortex: 1.8 nTPM
Single-cell type
- late primary spermatocytes: 877 nCPM
- early spermatids: 441 nCPM
- early primary spermatocytes: 398 nCPM
- differentiating spermatogonia: 145 nCPM
- late spermatids: 66 nCPM
- undifferentiated spermatogonia: 20 nCPM
Immune cell
- neutrophil: 4.4 nTPM
- myeloid DC: 1.1 nTPM
- eosinophil: 0.8 nTPM
- classical monocyte: 0.7 nTPM
- intermediate monocyte: 0.6 nTPM
- non-classical monocyte: 0.5 nTPM
Brain region
- medulla oblongata: 1.6 nTPM
- midbrain: 1.4 nTPM
- thalamus: 1.1 nTPM
- hypothalamus: 0.9 nTPM
- white matter: 0.9 nTPM
- cerebral cortex: 0.8 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)
- 1.02
- gnomAD pLI
- 0.6
- gnomAD missense Z
- 0.74
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- none
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
- apoptotic process
- cell division
- ectopic germ cell programmed cell death
- positive regulation of apoptotic process
- positive regulation of developmental process
- positive regulation of reproductive process
- reciprocal meiotic recombination
- spermatogenesis
- synaptonemal complex assembly
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Synaptonemal complex central element protein 3
- Synaptonemal complex central element protein 3
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SYCE3 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 SYCE3 as an antibody target. Whether an autoantibody or antibody against SYCE3 could matter depends on whether native SYCE3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SYCE3 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 SYCE3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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