ZSCAN1
Zinc finger and SCAN domain-containing protein 1
Also known as: FLJ33779, ZNF915, ZSCA1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NBB4
- Gene
- ZSCAN1
- Ensembl
- ENSG00000152467
- Chromosome
- 19
- Canonical length
- 408 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Nucleoli
OverviewNCBI Gene
Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
408 residues, UniProt reviewed canonical sequence.
>Q8NBB4|ZSCAN1
1 MLPRPKAPAS PRRPQTPTPS EQDADPGPAS PRDTEAQRLR FRQFQYHVAS GPHLALGQLW
61 TLCRQWLRPE ARSKEQMLEL LVLEQFLGAL PSKMRTWVQS QGPRSCREAA SLVEDLTQMC
121 QQEVLVSLDS VEPQDWSFGE EEDGKSPRSQ KEPSQASELI LDAVAAAPAL PEESEWLETT
181 QLQQSLHTRA EAEAPRAPGL LGSRARLPLK PSIWDEPEDL LAGPSSDLRA EGTVISSPKG
241 PSAQRISPRR RNRNTDQSGR HQPSLKHTKG GTQEAVAGIS VVPRGPRGGR PFQCADCGMV
301 FTWVTHFIEH QKTHREEGPF PCPECGKVFL HNSVLTEHGK IHLLEPPRKK APRSKGPRES
361 VPPRDGAQGP VAPRSPKRPF QCSVCGKAFP WMVHLIDHQK LHTAHGHMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZSCAN1 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)
- 0.55
- Highest tissue expression
- 16 nTPM
Expression across tissuesHPA
Tissue
- pituitary gland: 16 nTPM
- hypothalamus: 10 nTPM
- testis: 8.3 nTPM
- cerebral cortex: 7.4 nTPM
- choroid plexus: 7.4 nTPM
- amygdala: 7.1 nTPM
Single-cell type
- epididymal principal cells: 115 nCPM
- late spermatids: 74 nCPM
- late primary spermatocytes: 58 nCPM
- epididymal efferent duct ciliated cells: 48 nCPM
- fallopian tube ciliated cells: 43 nCPM
- early spermatids: 43 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- hypothalamus: 24 nTPM
- midbrain: 19 nTPM
- medulla oblongata: 16 nTPM
- cerebellum: 16 nTPM
- basal ganglia: 15 nTPM
- hippocampal formation: 15 nTPM
ReferencesPubMed · IEDB
Publications for ZSCAN1 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
5 publications
- ZSCAN1 Autoantibodies Are Associated with Pediatric Paraneoplastic ROHHAD.
2022 · Ann Neurol · RCR 4.2 · 48 citations - Antibodies Against ZSCAN1 in Pediatric and Adult Patients With Non-Paraneoplastic ROHHAD Syndrome.
2024 · Neurol Neuroimmunol Neuroinflamm · RCR 2.6 · 12 citations - Anti-ZSCAN1 Autoantibodies Are a Feasible Diagnostic Marker for ROHHAD Syndrome Not Associated with a Tumor.
2024 · Int J Mol Sci · RCR 2.5 · 11 citations - Autoimmunity related to anti-Nax and anti-ZSCAN1 autoantibodies in adipsic hypernatremia.
2024 · Endocr J · RCR 1 · 3 citations - Clinical characteristics and anti-ZSCAN1 antibody titer analysis in a nationwide survey of ROHHAD (-NET) syndrome.
2026 · J Clin Endocrinol Metab
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
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)
- 1.59
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.01
- DepMap mean gene effect
- 0.09
- 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
Molecular functions
- DNA-binding transcription factor activity, RNA polymerase II-specific
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- sequence-specific double-stranded DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZSCAN1 as an antibody target. Whether an autoantibody or antibody against ZSCAN1 could matter depends on whether native ZSCAN1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZSCAN1 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 ZSCAN1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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