ZNF596
Zinc finger protein 596
Also known as: ZN596_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TC21
- Gene
- ZNF596
- Ensembl
- ENSG00000172748
- Chromosome
- 8
- Canonical length
- 504 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoli,Mitochondria
OverviewNCBI Gene
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
504 residues, UniProt reviewed canonical sequence.
>Q8TC21|ZNF596
1 MPSPDSMTFE DIIVDFTQEE WALLDTSQRK LFQDVMLENI SHLVSIGKQL CKSVVLSQLE
61 QVEKLSTQRI SLLQGREVGI KHQEIPFIQH IYQKGTSTIS TMRSHTQEDP FLCNDLGEDF
121 TQHIALTQNV ITYMRTKHFV SKKFGKIFSD WLSFNQHKEI HTKCKSYGSH LFDYAFIQNS
181 ALRPHSVTHT REITLECRVC GKTFSKNSNL RRHEMIHTGE KPHGCHLCGK AFTHCSDLRK
241 HERTHTGEKP YGCHLCGKAF SKSSNLRRHE MIHTREKAQI CHLCGKAFTH CSDLRKHERT
301 HLGDKPYGCL LCGKAFSKCS YLRQHERTHN GEKPYECHLC GKAFSHCSHL RQHERSHNGE
361 KPHGCHLCGK AFTESSVLKR HERIHTGEKP YECHVCGKAF TESSDLRRHE RTHTGEKPYE
421 CHLCGKAFNH SSVLRRHERT HTGEKPYECN ICGKAFNRSY NFRLHRRVHT GEKPYVCPLC
481 GKAFSKFFNL RQHERTHTKK AMNMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF596 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)
- 0.42
- Highest tissue expression
- 17 nTPM
Expression across tissuesHPA
Tissue
- retina: 17 nTPM
- testis: 15 nTPM
- cerebellum: 9.4 nTPM
- endometrium: 6.6 nTPM
- epididymis: 6.6 nTPM
- thyroid gland: 5.4 nTPM
Single-cell type
- epicardial cells: 200 nCPM
- late primary spermatocytes: 131 nCPM
- cardiomyocytes: 81 nCPM
- early spermatids: 47 nCPM
- mesothelial cells: 39 nCPM
- sertoli cells: 30 nCPM
Immune cell
- basophil: 4.7 nTPM
- naive B-cell: 3.6 nTPM
- naive CD8 T-cell: 3.4 nTPM
- memory B-cell: 3.2 nTPM
- MAIT T-cell: 3.1 nTPM
- naive CD4 T-cell: 2.9 nTPM
Brain region
- cerebellum: 19 nTPM
- white matter: 16 nTPM
- hypothalamus: 13 nTPM
- cerebral cortex: 12 nTPM
- choroid plexus: 11 nTPM
- thalamus: 11 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)
- 1.54
- gnomAD pLI
- 0
- gnomAD missense Z
- -2.55
- DepMap mean gene effect
- 0.1
- 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
- DNA-binding transcription factor activity, RNA polymerase II-specific
- RNA polymerase II transcription regulatory region sequence-specific DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZNF596 as an antibody target. Whether an autoantibody or antibody against ZNF596 could matter depends on whether native ZNF596 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF596 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 ZNF596 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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