ZNF439
Zinc finger protein 439
Also known as: DKFZp571K0837, ZN439_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NDP4
- Gene
- ZNF439
- Ensembl
- ENSG00000171291
- Chromosome
- 19
- Canonical length
- 499 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
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
499 residues, UniProt reviewed canonical sequence.
>Q8NDP4|ZNF439
1 MLSLSPILLY TCEMFQDPVA FKDVAVNFTQ EEWALLDISQ KNLYREVMLE TFWNLTSIGK
61 KWKDQNIEYE YQNPRRNFRS VTEEKVNEIK EDSHCGETFT PVPDDRLNFQ KKKASPEVKS
121 CDSFVCEVGL GNSSSNMNIR GDTGHKACEC QEYGPKPWKS QQPKKAFRYH PSLRTQERDH
181 TGKKPYACKE CGKNIIYHSS IQRHMVVHSG DGPYKCKFCG KAFHCLSLYL IHERTHTGEK
241 PYECKQCGKS FSYSATHRIH ERTHIGEKPY ECQECGKAFH SPRSCHRHER SHMGEKAYQC
301 KECGKAFMCP RYVRRHERTH SRKKLYECKQ CGKALSSLTS FQTHIRMHSG ERPYECKTCG
361 KGFYSAKSFQ RHEKTHSGEK PYKCKQCGKA FTRSGSFRYH ERTHTGEKPY ECKQCGKAFR
421 SAPNLQLHGR THTGEKPYQC KECGKAFRSA SQLRIHRRIH TGEKPYECKK CGKAFRYVQN
481 FRFHERTQTH KNALWRKTLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF439 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)
- 0.47
- Highest tissue expression
- 16 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 16 nTPM
- retina: 14 nTPM
- cerebellum: 9.9 nTPM
- thymus: 9.6 nTPM
- pituitary gland: 8.6 nTPM
- spleen: 7.8 nTPM
Single-cell type
- hematopoietic stem cells: 69 nCPM
- cytotrophoblasts: 62 nCPM
- thymocytes: 58 nCPM
- mast cells: 55 nCPM
- choroid plexus epithelial cells: 54 nCPM
- podocytes: 52 nCPM
Immune cell
- basophil: 24 nTPM
- memory B-cell: 7.7 nTPM
- naive B-cell: 7.1 nTPM
- eosinophil: 5 nTPM
- naive CD4 T-cell: 4.6 nTPM
- non-classical monocyte: 3.2 nTPM
Brain region
- cerebellum: 18 nTPM
- white matter: 14 nTPM
- pons: 11 nTPM
- medulla oblongata: 11 nTPM
- basal ganglia: 10 nTPM
- cerebral cortex: 10 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)
- 1.69
- gnomAD pLI
- 0.01
- gnomAD missense Z
- -0.48
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% 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
InteractionsUniProt · HPA
Protein binding partners of ZNF439 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 ZNF439 as an antibody target. Whether an autoantibody or antibody against ZNF439 could matter depends on whether native ZNF439 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF439 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 ZNF439 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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