ZNF768
Zinc finger protein 768
Also known as: FLJ23436, ZN768_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H5H4
- Gene
- ZNF768
- Ensembl
- ENSG00000169957
- Chromosome
- 16
- Canonical length
- 540 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Vesicles
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 chromosome. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
540 residues, UniProt reviewed canonical sequence.
>Q9H5H4|ZNF768
1 MEREALPWGL EPQDVQSSDE MRSPEGYLRG NMSENEEEEI SQQEGSGDYE VEEIPFGLEP
61 QSPGFEPQSP EFEPQSPRFE PESPGFESRS PGLVPPSPEF APRSPESDSQ SPEFESQSPR
121 YEPQSPGYEP RSPGYEPRSP GYESESSRYE SQNTELKTQS PEFEAQSSKF QEGAEMLLNP
181 EEKSPLNISV GVHPLDSFTQ GFGEQPTGDL PIGPPFEMPT GALLSTPQFE MLQNPLGLTG
241 ALRGPGRRGG RARGGQGPRP NICGICGKSF GRGSTLIQHQ RIHTGEKPYK CEVCSKAFSQ
301 SSDLIKHQRT HTGERPYKCP RCGKAFADSS YLLRHQRTHS GQKPYKCPHC GKAFGDSSYL
361 LRHQRTHSHE RPYSCTECGK CYSQNSSLRS HQRVHTGQRP FSCGICGKSF SQRSALIPHA
421 RSHAREKPFK CPECGKRFGQ SSVLAIHART HLPGRTYSCP DCGKTFNRSS TLIQHQRSHT
481 GERPYRCAVC GKGFCRSSTL LQHHRVHSGE RPYKCDDCGK AFSQSSDLIR HQRTHAAGRRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF768 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)
- 0.54
- Highest tissue expression
- 88 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 88 nTPM
- tongue: 50 nTPM
- heart muscle: 46 nTPM
- colon: 41 nTPM
- testis: 38 nTPM
- liver: 37 nTPM
Single-cell type
- colonocytes: 48 nCPM
- enterocytes: 37 nCPM
- late primary spermatocytes: 31 nCPM
- goblet cells: 29 nCPM
- enteric stem cells: 28 nCPM
- enteric transient amplifying cells: 25 nCPM
Immune cell
- memory B-cell: 1.1 nTPM
- eosinophil: 1 nTPM
- intermediate monocyte: 0.6 nTPM
- myeloid DC: 0.6 nTPM
- NK-cell: 0.6 nTPM
- neutrophil: 0.5 nTPM
Brain region
- thalamus: 41 nTPM
- basal ganglia: 40 nTPM
- midbrain: 38 nTPM
- medulla oblongata: 38 nTPM
- amygdala: 37 nTPM
- cerebellum: 35 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)
- 0.5
- gnomAD pLI
- 0.42
- gnomAD missense Z
- 2.72
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
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 binding
- RNA polymerase II transcription regulatory region sequence-specific DNA binding
- sequence-specific double-stranded DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ZNF768 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 ZNF768 as an antibody target. Whether an autoantibody or antibody against ZNF768 could matter depends on whether native ZNF768 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF768 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 ZNF768 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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