ZNF764
Zinc finger protein 764
Also known as: MGC13138, ZN764_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96H86
- Gene
- ZNF764
- Ensembl
- ENSG00000169951
- Chromosome
- 16
- Canonical length
- 408 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Cytosol
OverviewNCBI Gene
Enables transcription coregulator activity. Involved in cellular response to glucocorticoid stimulus. Is active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
408 residues, UniProt reviewed canonical sequence.
>Q96H86|ZNF764
1 MAPPLAPLPP RDPNGAGPEW REPGAVSFAD VAVYFCREEW GCLRPAQRAL YRDVMRETYG
61 HLSALGIGGN KPALISWVEE EAELWGPAAQ DPEVAKCQTQ TDPADSRNKK KERQREGTGA
121 LEKPDPVAAG SPGLKSPQAP SAGPPYGWEQ LSKAPHRGRP SLCAHPPVPR ADQRHGCYVC
181 GKSFAWRSTL VEHVYSHTGE KPFHCTDCGK GFGHASSLSK HRAIHRGERP HRCLECGRAF
241 TQRSALTSHL RVHTGEKPYG CADCGRRFSQ SSALYQHRRV HSGETPFPCP DCGRAFAYPS
301 DLRRHVRTHT GEKPYPCPDC GRCFRQSSEM AAHRRTHSGE KPYPCPQCGR RFGQKSAVAK
361 HQWVHRPGAG GHRGRVAGRL SVTLTPGHGD LDPPVGFQLY PEIFQECGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF764 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)
- 0.5
- Highest tissue expression
- 6.5 nTPM
Expression across tissuesHPA
Tissue
- stomach: 6.5 nTPM
- heart muscle: 6.3 nTPM
- liver: 5.7 nTPM
- testis: 5.6 nTPM
- ovary: 5.5 nTPM
- spleen: 5 nTPM
Single-cell type
- tuft cells: 23 nCPM
- retinal pigment epithelial cells: 13 nCPM
- early primary spermatocytes: 12 nCPM
- erythrocyte progenitors: 12 nCPM
- fallopian tube ciliated cells: 9.9 nCPM
- granulosa cells: 9.7 nCPM
Immune cell
- NK-cell: 7.2 nTPM
- eosinophil: 4.4 nTPM
- MAIT T-cell: 3.9 nTPM
- memory CD8 T-cell: 3.7 nTPM
- naive CD4 T-cell: 3.1 nTPM
- memory CD4 T-cell: 3 nTPM
Brain region
- cerebellum: 15 nTPM
- cerebral cortex: 11 nTPM
- white matter: 11 nTPM
- hypothalamus: 11 nTPM
- hippocampal formation: 11 nTPM
- medulla oblongata: 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)
- 1.17
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.45
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% 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
- transcription coregulator activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ZNF764 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 ZNF764 as an antibody target. Whether an autoantibody or antibody against ZNF764 could matter depends on whether native ZNF764 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF764 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 ZNF764 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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