ZNF232
Zinc finger protein 232
Also known as: ZN232_HUMAN, ZSCAN11
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UNY5
- Gene
- ZNF232
- Ensembl
- ENSG00000167840
- Chromosome
- 17
- Canonical length
- 444 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Vesicles,Cytosol
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. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
444 residues, UniProt reviewed canonical sequence.
>Q9UNY5|ZNF232
1 MEPPGPVRGP LQDSSWYEPS AELVQTRMAV SLTAAETLAL QGTQGQEKMM MMGPKEEEQS
61 CEYETRLPGN HSTSQEIFRQ RFRHLRYQET PGPREALSQL RVLCCEWLRP EKHTKEQILE
121 FLVLEQFLTI LPEELQSWVR GHHPKSGEEA VTVLEDLEKG LEPEPQVPGP AHGPAQEEPW
181 EKKESLGAAQ EALSIQLQPK ETQPFPKSEQ VYLHFLSVVT EDGPEPKDKG SLPQPPITEV
241 ESQVFSEKLA TDTSTFEATS EGTLELQQRN PKAERLRWSP AQEESFRQMV VIHKEIPTGK
301 KDHECSECGK TFIYNSHLVV HQRVHSGEKP YKCSDCGKTF KQSSNLGQHQ RIHTGEKPFE
361 CNECGKAFRW GAHLVQHQRI HSGEKPYECN ECGKAFSQSS YLSQHRRIHS GEKPFICKEC
421 GKAYGWCSEL IRHRRVHARK EPSHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF232 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
- 9 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 9 nTPM
- ovary: 7.4 nTPM
- fallopian tube: 5.7 nTPM
- retina: 5.5 nTPM
- smooth muscle: 5.4 nTPM
- tonsil: 5.4 nTPM
Single-cell type
- early primary spermatocytes: 39 nCPM
- respiratory ciliated cells: 29 nCPM
- cardiomyocytes: 29 nCPM
- differentiating spermatogonia: 22 nCPM
- oocytes: 18 nCPM
- fallopian tube ciliated cells: 18 nCPM
Immune cell
- memory B-cell: 6 nTPM
- intermediate monocyte: 5.5 nTPM
- naive B-cell: 5.4 nTPM
- MAIT T-cell: 4.8 nTPM
- myeloid DC: 4.1 nTPM
- naive CD4 T-cell: 3.7 nTPM
Brain region
- choroid plexus: 8.3 nTPM
- cerebellum: 7.1 nTPM
- white matter: 6.9 nTPM
- hypothalamus: 5.6 nTPM
- thalamus: 5.6 nTPM
- cerebral cortex: 5.4 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)
- 0.93
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.27
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- none
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 cis-regulatory region sequence-specific DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ZNF232 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 ZNF232 as an antibody target. Whether an autoantibody or antibody against ZNF232 could matter depends on whether native ZNF232 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF232 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 ZNF232 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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