SYNC
Syncoilin
Also known as: SYNC1, SYNCI_HUMAN, SYNCOILIN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H7C4
- Gene
- SYNC
- Ensembl
- ENSG00000162520
- Chromosome
- 1
- Canonical length
- 482 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Golgi apparatus,Vesicles,Plasma membrane
OverviewNCBI Gene
This gene encodes a member of the intermediate filament family which contains an N-terminal head domain, followed by a central coiled-coil region and a short C-terminal tail. The protein is highly expressed in skeletal and cardiac muscle. The protein links the dystrophin associated protein complex (DAPC) to desmin filaments in muscle and may have a structural role in striated muscle. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2009]
Canonical amino-acid sequenceUniProt
482 residues, UniProt reviewed canonical sequence.
>Q9H7C4|SYNC
1 MASPEPRRGG DGAAQAARKT RVEANSPLPK NSGSLNEAEA LNPEVTLSSE GSLNLEDILY
61 LEDTGDLDET LYVQETEKAE EALYIEEAMQ PDEALHVEEP GNPEETVCVE ETTEPDRIQF
121 VEGPVEPGKP TSPEHVVYEG ETVTRAEKSN PEESLRAEQS PSMEENLSIE DLELLEGRFQ
181 QCVQAVAQLE EERDQLIHEL VLLREPALQE VQQVHQDILA AYKLHAQAEL ERDGLREEIR
241 LVKQKLFKVT KECVAYQYQL ECRQQDVAQF ADFREVLTTR ATQLSEELAQ LRDAYQKQKE
301 QLRQQLEAPP SQRDGHFLQE SRRLSAQFEN LMAESRQDLE EEYEPQFLRL LERKEAGTKA
361 LQRTQAEIQE MKEALRPLQA EARQLRLQNR NLEDQIALVR QKRDEEVQQY REQLEEMEER
421 QRQLRNGVQL QQQKNKEMEQ LRLSLAEELS TYKAMLLPKS LEQADAPTSQ AGGMETQSQG
481 AVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SYNC 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)
- 0.58
- Highest tissue expression
- 100 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 100 nTPM
- tongue: 69 nTPM
- smooth muscle: 50 nTPM
- blood vessel: 27 nTPM
- esophagus: 17 nTPM
- heart muscle: 16 nTPM
Single-cell type
- thymic myoid cells: 158 nCPM
- myonuclei: 146 nCPM
- peritubular myoid cells: 85 nCPM
- sertoli cells: 65 nCPM
- differentiating spermatogonia: 64 nCPM
- leydig cells: 63 nCPM
Immune cell
- plasmacytoid DC: 12 nTPM
- total PBMC: 12 nTPM
- myeloid DC: 9.7 nTPM
- intermediate monocyte: 9.6 nTPM
- non-classical monocyte: 9.6 nTPM
- NK-cell: 9.2 nTPM
Brain region
- spinal cord: 17 nTPM
- midbrain: 16 nTPM
- medulla oblongata: 15 nTPM
- white matter: 14 nTPM
- hypothalamus: 14 nTPM
- thalamus: 13 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)
- 0.87
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.67
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- intermediate filament-based process
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SYNC 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 SYNC as an antibody target. Whether an autoantibody or antibody against SYNC could matter depends on whether native SYNC is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SYNC 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 SYNC as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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