ZFP92
Zinc finger protein 92 homolog
Also known as: ZFP92_HUMAN, ZNF897
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A6NM28
- Gene
- ZFP92
- Ensembl
- ENSG00000189420
- Chromosome
- X
- Canonical length
- 416 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
OverviewNCBI Gene
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-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, Apr 2025]
Canonical amino-acid sequenceUniProt
416 residues, UniProt reviewed canonical sequence.
>A6NM28|ZFP92
1 MAAILLTTRP KVPVSFEDVS VYFTKTEWKL LDLRQKVLYK RVMLENYSHL VSLGFSFSKP
61 HLISQLERGE GPWVADIPRT WATAGLHIGD RTQSKTSTST QKHSGRQLPG ADPQGGKEGQ
121 AARSSVLQRG AQGLGQSSAA GPQGPKGAEK RYLCQQCGKA FSRSSNLIKH RIIHSGEKPY
181 ACPECGKLFR RSFALLEHQR IHSGEKPYAC PECSKTFTRS SNLIKHQVIH SGERPFACGD
241 CGKLFRRSFA LLEHARVHSG ERPYACPECG KAFSRSSNLI EHQRTHRGEK PYACGQCAKA
301 FKGVSQLIHH QRSHSGERPF ACRECGKAFR GRSGLSQHRR VHSGEKPYEC SDCGKAFGRR
361 ANLFKHQAVH GARRPAKAET ARRLAGPGST GPGSAVAATS PPRPSTAARP SRPSRRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZFP92 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)
- 0.49
- Highest tissue expression
- 3.9 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 3.9 nTPM
- ovary: 3.7 nTPM
- cerebellum: 3.2 nTPM
- fallopian tube: 2.9 nTPM
- bone marrow: 2.7 nTPM
- pituitary gland: 2.4 nTPM
Single-cell type
- gonadotrophs: 12 nCPM
- endometrial luminal cells: 8.2 nCPM
- neutrophil progenitors: 8 nCPM
- pericytes: 7.9 nCPM
- decidual stromal cells: 7.5 nCPM
- megakaryocytes: 6.2 nCPM
Immune cell
- intermediate monocyte: 0.2 nTPM
- gdT-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- hypothalamus: 7.5 nTPM
- cerebellum: 7.4 nTPM
- choroid plexus: 7.4 nTPM
- thalamus: 7 nTPM
- basal ganglia: 6.5 nTPM
- pons: 6.4 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)
- 0.62
- gnomAD pLI
- 0.65
- gnomAD missense Z
- 2.05
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of transcription by RNA polymerase II
- regulation of glucose metabolic process
- regulation of lipid metabolic process
- regulation of transcription by RNA polymerase II
- transposable element silencing
Molecular functions
- DNA-binding transcription factor activity, RNA polymerase II-specific
- DNA-binding transcription repressor activity, RNA polymerase II-specific
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZFP92 as an antibody target. Whether an autoantibody or antibody against ZFP92 could matter depends on whether native ZFP92 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZFP92 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 ZFP92 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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