ZSWIM7
Zinc finger SWIM domain-containing protein 7
Also known as: SWS1, ZSWM7_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q19AV6
- Gene
- ZSWIM7
- Ensembl
- ENSG00000214941
- Chromosome
- 17
- Canonical length
- 140 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Predicted to enable zinc ion binding activity. Involved in double-strand break repair via homologous recombination and protein stabilization. Part of Shu complex. Implicated in ovarian dysgenesis 10 and spermatogenic failure 71. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
140 residues, UniProt reviewed canonical sequence.
>Q19AV6|ZSWIM7
1 MAVVLPAVVE ELLSEMAAAV QESARIPDEY LLSLKFLFGS SATQALDLVD RQSITLISSP
61 SGRRVYQVLG SSSKTYTCLA SCHYCSCPAF AFSVLRKSDS ILCKHLLAVY LSQVMRTCQQ
121 LSVSDKQLTD ILLMEKKQEALocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZSWIM7 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
- 31 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 31 nTPM
- midbrain: 17 nTPM
- heart muscle: 17 nTPM
- adrenal gland: 17 nTPM
- choroid plexus: 17 nTPM
- cerebral cortex: 16 nTPM
Single-cell type
- cytotrophoblasts: 153 nCPM
- platelets: 131 nCPM
- early primary spermatocytes: 120 nCPM
- megakaryocytes: 105 nCPM
- syncytiotrophoblasts: 94 nCPM
- ovarian stromal cells: 90 nCPM
Immune cell
- myeloid DC: 42 nTPM
- basophil: 28 nTPM
- intermediate monocyte: 28 nTPM
- classical monocyte: 27 nTPM
- memory B-cell: 27 nTPM
- plasmacytoid DC: 26 nTPM
Brain region
- cerebral cortex: 11 nTPM
- hypothalamus: 9.5 nTPM
- pons: 9 nTPM
- medulla oblongata: 8.7 nTPM
- hippocampal formation: 8.6 nTPM
- white matter: 8.5 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about ZSWIM7.
Disease | AllUniProt
Conditions ZSWIM7 is implicated in, by any mechanism.
- Ovarian dysgenesis 10 (ODG10) MIM:619834
- Spermatogenic failure 71 (SPGF71) MIM:619831
Disease | GeneticClinVar
4 pathogenic / likely-pathogenic of 34 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Spermatogenic failure 71
- Ovarian dysgenesis 10
- Non-obstructive azoospermia
- Infertility disorder
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)
- 1.21
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.33
- DepMap mean gene effect
- -0.05
- 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 ZSWIM7 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 ZSWIM7 as an antibody target. Whether an autoantibody or antibody against ZSWIM7 could matter depends on whether native ZSWIM7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZSWIM7 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 ZSWIM7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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