ZNF226
Zinc finger protein 226
Also known as: ZN226_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NYT6
- Gene
- ZNF226
- Ensembl
- ENSG00000167380
- Chromosome
- 19
- Canonical length
- 803 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nuclear bodies
OverviewNCBI Gene
Predicted to enable DNA binding activity and zinc ion 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, Jul 2025]
Canonical amino-acid sequenceUniProt
803 residues, UniProt reviewed canonical sequence.
>Q9NYT6|ZNF226
1 MNMFKEAVTF KDVAVAFTEE ELGLLGPAQR KLYRDVMVEN FRNLLSVGHP PFKQDVSPIE
61 RNEQLWIMTT ATRRQGNLGE KNQSKLITVQ DRESEEELSC WQIWQQIAND LTRCQDSMIN
121 NSQCHKQGDF PYQVGTELSI QISEDENYIV NKADGPNNTG NPEFPILRTQ DSWRKTFLTE
181 SQRLNRDQQI SIKNKLCQCK KGVDPIGWIS HHDGHRVHKS EKSYRPNDYE KDNMKILTFD
241 HNSMIHTGQK SYQCNECKKP FSDLSSFDLH QQLQSGEKSL TCVERGKGFC YSPVLPVHQK
301 VHVGEKLKCD ECGKEFSQGA HLQTHQKVHV IEKPYKCKQC GKGFSRRSAL NVHCKVHTAE
361 KPYNCEECGR AFSQASHLQD HQRLHTGEKP FKCDACGKSF SRNSHLQSHQ RVHTGEKPYK
421 CEECGKGFIC SSNLYIHQRV HTGEKPYKCE ECGKGFSRPS SLQAHQGVHT GEKSYICTVC
481 GKGFTLSSNL QAHQRVHTGE KPYKCNECGK SFRRNSHYQV HLVVHTGEKP YKCEICGKGF
541 SQSSYLQIHQ KAHSIEKPFK CEECGQGFNQ SSRLQIHQLI HTGEKPYKCE ECGKGFSRRA
601 DLKIHCRIHT GEKPYNCEEC GKVFRQASNL LAHQRVHSGE KPFKCEECGK SFGRSAHLQA
661 HQKVHTGDKP YKCDECGKGF KWSLNLDMHQ RVHTGEKPYK CGECGKYFSQ ASSLQLHQSV
721 HTGEKPYKCD VCGKVFSRSS QLQSHQRVHT GEKPYKCEIC GKSFSWRSNL TVHHRIHVGD
781 KSYKSNRGGK NIRESTQEKK SIKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF226 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
- 40 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 40 nTPM
- pituitary gland: 31 nTPM
- adrenal gland: 30 nTPM
- retina: 29 nTPM
- midbrain: 26 nTPM
- epididymis: 24 nTPM
Single-cell type
- epididymal principal cells: 70 nCPM
- retinal pigment epithelial cells: 60 nCPM
- esophageal apical cells: 56 nCPM
- epididymal clear cells: 51 nCPM
- cardiomyocytes: 47 nCPM
- gastric progenitor cells: 45 nCPM
Immune cell
- basophil: 54 nTPM
- naive B-cell: 28 nTPM
- T-reg: 27 nTPM
- NK-cell: 27 nTPM
- naive CD4 T-cell: 26 nTPM
- MAIT T-cell: 25 nTPM
Brain region
- white matter: 61 nTPM
- cerebellum: 57 nTPM
- cerebral cortex: 50 nTPM
- choroid plexus: 48 nTPM
- hypothalamus: 48 nTPM
- basal ganglia: 48 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)
- 1.16
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.83
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% 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 transcription by RNA polymerase II
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZNF226 as an antibody target. Whether an autoantibody or antibody against ZNF226 could matter depends on whether native ZNF226 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF226 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 ZNF226 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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