ZNF17
Zinc finger protein 17
Also known as: FLJ40864, FLJ46058, FLJ46615, HPF3, KIAA1947, KOX10, ZNF17_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P17021
- Gene
- ZNF17
- Ensembl
- ENSG00000186272
- Chromosome
- 19
- Canonical length
- 662 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, Jul 2025]
Canonical amino-acid sequenceUniProt
662 residues, UniProt reviewed canonical sequence.
>P17021|ZNF17
1 MNLTEDYMVF EDVAIHFSQE EWGILNDVQR HLHSDVMLEN FALLSSVGCW HGAKDEEAPS
61 KQCVSVGVSQ VTTLKPALST QKAQPCETCS SLLKDILHLA EHDGTHPKRT AKLYLHQKEH
121 LREKLTRSDE GRPSFVNDSV HLAKRNLTCM QGGKDFTGDS DLQQQALHSG WKPHRDTHGV
181 EAFQSGQNNY SCTQCGKDFC HQHTLFEHQK IHTEERPYEC SECGKLFRYN SDLIKHQRNH
241 TGERPYKCSE CGKAFSLKYN VVQHQKIHTG ERPYECSECG KAFLRKSHLL QHQRIHTRPR
301 PYVCSECGKA FLTQAHLVGH QKIHTGERPY GCNECGKYFM YSSALIRHQK VHTGERPFYC
361 CECGKFFMDS CTLIIHQRVH TGEKPYECNE CGKFFRYRST LIRHQKVHTG EKPYECSECG
421 KFFMDTSTLI IHQRVHTGEK PYECNKCGKF FRYCFTLNRH QRVHSGERPY ECSECGKFFV
481 DSCTLKSHQR VHTGERPFEC SICGKSFRCR STLDTHQRIH TGERPYECSE CGKFFRHNSN
541 HIRHRRNHFG ERSFECTECG RVFSQNSHLI RHQKVHTRER TYKCSKCGKF FMDSSTLISH
601 ERVHTGEKPY ECSECGKVFR YNSSLIKHRR IHTGERPYQC SECGRVFNQN SHLIQHQKVH
661 TRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF17 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)
- 0.43
- Highest tissue expression
- 8.1 nTPM
Expression across tissuesHPA
Tissue
- retina: 8.1 nTPM
- tongue: 5.9 nTPM
- ovary: 5.6 nTPM
- thymus: 5.6 nTPM
- breast: 5 nTPM
- thyroid gland: 4.8 nTPM
Single-cell type
- adipocytes: 0.8 nCPM
- thymocytes: 0.8 nCPM
- prostatic club cells: 0.5 nCPM
- cardiomyocytes: 0.4 nCPM
- basal prostatic cells: 0.3 nCPM
- fibro-adipogenic progenitors: 0.3 nCPM
Immune cell
- NK-cell: 6.4 nTPM
- naive CD4 T-cell: 5.8 nTPM
- MAIT T-cell: 5.1 nTPM
- memory CD8 T-cell: 5.1 nTPM
- naive B-cell: 4.7 nTPM
- memory CD4 T-cell: 4.5 nTPM
Brain region
- cerebellum: 23 nTPM
- white matter: 19 nTPM
- cerebral cortex: 18 nTPM
- basal ganglia: 16 nTPM
- hippocampal formation: 16 nTPM
- amygdala: 16 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)
- 1.4
- gnomAD pLI
- 0.23
- gnomAD missense Z
- 0.48
- DepMap mean gene effect
- -0.01
- 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 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 ZNF17 as an antibody target. Whether an autoantibody or antibody against ZNF17 could matter depends on whether native ZNF17 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF17 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 ZNF17 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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