ZNF253
Zinc finger protein 253
Also known as: BMZF-1, FLJ90391, ZN253_HUMAN, ZNF411
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75346
- Gene
- ZNF253
- Ensembl
- ENSG00000256771
- Chromosome
- 19
- Canonical length
- 499 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 DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
499 residues, UniProt reviewed canonical sequence.
>O75346|ZNF253
1 MGPLQFRDVA IEFSLEEWHC LDTAQRNLYR DVMLENYRNL VFLGIVVSKP DLVTCLEQGK
61 KPLTMERHEM IAKPPVMSSH FAQDLWPENI QNSFQIGMLR RYEECRHDNL QLKKGCKSVG
121 EHKVHKGGYN GLNQCLTTTQ KEIFQCDKYG KVFHKFSNSN TYKTRHTGIN LFKCIICGKA
181 FKRSSTLTTH KKIHTGEKPY RCEECGKAFN QSANLTTHKR IHTGEKPYRC EECGKAFKQS
241 SNLTTHKKIH TGEKPYKCEE CGKAFNRSTD LTTHKIVHTG EKPYKCEECG KAFKHPSHVT
301 THKKIHTRGK PYNCEECGKS FKHCSNLTIH KRIHTGEKPY KCEECGKAFH LSSHLTTHKI
361 LHTGEKPYRC RECGKAFNHS TTLFSHEKIH TGEKPYKCDE CGKTFTWPSI LSKHKRTHTG
421 EKPYKCEECG KSFTASSTLT THKRIHTGEK PYKCEECGKA FNWSSDLNKH KKIHIERKPY
481 IVKNVTDLLN VPPLLISIRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF253 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
- 18 nTPM
Expression across tissuesHPA
Tissue
- retina: 18 nTPM
- thyroid gland: 14 nTPM
- ovary: 12 nTPM
- tongue: 9.8 nTPM
- thymus: 8.4 nTPM
- lymph node: 8 nTPM
Single-cell type
- myonuclei: 113 nCPM
- rod photoreceptor cells: 113 nCPM
- cardiomyocytes: 73 nCPM
- corticotrophs: 70 nCPM
- oligodendrocytes: 51 nCPM
- lactotrophs: 42 nCPM
Immune cell
- naive CD4 T-cell: 15 nTPM
- basophil: 13 nTPM
- naive CD8 T-cell: 10 nTPM
- naive B-cell: 9.4 nTPM
- memory B-cell: 9 nTPM
- memory CD8 T-cell: 7.7 nTPM
Brain region
- cerebellum: 29 nTPM
- white matter: 22 nTPM
- hypothalamus: 22 nTPM
- cerebral cortex: 21 nTPM
- basal ganglia: 19 nTPM
- thalamus: 18 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)
- 1.66
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.57
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
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
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
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZNF253 as an antibody target. Whether an autoantibody or antibody against ZNF253 could matter depends on whether native ZNF253 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF253 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 ZNF253 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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