ZBTB11
Zinc finger and BTB domain-containing protein 11
Also known as: ZBT11_HUMAN, ZNF-U69274, ZNF913
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95625
- Gene
- ZBTB11
- Ensembl
- ENSG00000066422
- Chromosome
- 3
- Canonical length
- 1053 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins, Predicted membrane proteins, Transcription factors
- Subcellular location
- Nucleoplasm
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. Located in nucleoplasm. Implicated in autosomal recessive intellectual developmental disorder 69. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1053 residues, UniProt reviewed canonical sequence.
>O95625|ZBTB11
1 MSSEESYRAI LRYLTNEREP YAPGTEGNVK RKIRKAAACY VVRGGTLYYQ RRQRHRKTFA
61 ELEVVLQPER RRDLIEAAHL GPGGTHHTRH QTWHYLSKTY WWRGILKQVK DYIKQCSKCQ
121 EKLDRSRPIS DVSEMLEELG LDLESGEESN ESEDDLSNFT SSPTTASKPA KKKPVSKHEL
181 VFVDTKGVVK RSSPKHCQAV LKQLNEQRLS NQFCDVTLLI EGEEYKAHKS VLSANSEYFR
241 DLFIEKGAVS SHEAVVDLSG FCKASFLPLL EFAYTSVLSF DFCSMADVAI LARHLFMSEV
301 LEICESVHKL MEEKQLTVYK KGEVQTVAST QDLRVQNGGT APPVASSEGT TTSLPTELGD
361 CEIVLLVNGE LPEAEQNGEV GRQPEPQVSS EAESALSSVG CIADSHPEME SVDLITKNNQ
421 TELETSNNRE NNTVSNIHPK LSKENVISSS PEDSGMGNDI SAEDICAEDI PKHRQKVDQP
481 LKDQENLVAS TAKTDFGPDD DTYRSRLRQR SVNEGAYIRL HKGMEKKLQK RKAVPKSAVQ
541 QVAQKLVQRG KKMKQPKRDA KENTEEASHK CGECGMVFQR RYALIMHKLK HERARDYKCP
601 LCKKQFQYSA SLRAHLIRHT RKDAPSSSSS NSTSNEASGT SSEKGRTKRE FICSICGRTL
661 PKLYSLRIHM LKHTGVKPHA CQVCGKTFIY KHGLKLHQSL HQSQKQFQCE LCVKSFVTKR
721 SLQEHMSIHT GESKYLCSVC GKSFHRGSGL SKHFKKHQPK PEVRGYHCTQ CEKSFFEARD
781 LRQHMNKHLG VKPFQCQFCD KCYSWKKDWY SHVKSHSVTE PYRCNICGKE FYEKALFRRH
841 VKKATHGKKG RAKQNLERVC EKCGRKFTQL REYRRHMNNH EGVKPFECLT CGVAWADARS
901 LKRHVRTHTG ERPYVCPVCS EAYIDARTLR KHMTKFHRDY VPCKIMLEKD TLQFHNQGTQ
961 VAHAVSILTA GMQEQESSGP QELETVVVTG ETMEALEAVA ATEEYPSVST LSDQSIMQVV
1021 NYVLAQQQGQ KLSEVAEAIQ TVKVEVAHIS GGELocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZBTB11 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)
- 0.51
- Highest tissue expression
- 15 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 15 nTPM
- pancreas: 8.3 nTPM
- skeletal muscle: 6.8 nTPM
- esophagus: 6.6 nTPM
- skin: 6.6 nTPM
- liver: 6.3 nTPM
Single-cell type
- neutrophil progenitors: 164 nCPM
- neutrophils: 141 nCPM
- endometrial glandular cells: 138 nCPM
- endometrial luminal cells: 133 nCPM
- monocyte progenitors: 127 nCPM
- endometrial stromal cells: 116 nCPM
Immune cell
- basophil: 4.7 nTPM
- non-classical monocyte: 4.5 nTPM
- eosinophil: 3.2 nTPM
- myeloid DC: 2.6 nTPM
- intermediate monocyte: 2.3 nTPM
- MAIT T-cell: 2.3 nTPM
Brain region
- cerebellum: 24 nTPM
- cerebral cortex: 21 nTPM
- white matter: 19 nTPM
- basal ganglia: 17 nTPM
- hypothalamus: 17 nTPM
- midbrain: 16 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about ZBTB11.
Disease | AllUniProt
Conditions ZBTB11 is implicated in, by any mechanism.
- Neurodevelopmental disorder with progressive movement abnormalities, cognitive decline, and brain abnormalities (NEDMCB) MIM:618383
Disease | GeneticClinVar
10 pathogenic / likely-pathogenic of 178 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Intellectual developmental disorder, autosomal recessive 69
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)
- 0.54
- gnomAD pLI
- 0
- gnomAD missense Z
- 2.05
- DepMap mean gene effect
- -1.25
- DepMap dependency class
- common
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
- BTB/POZ domain
- SKP1/BTB/POZ domain superfamily
- Zinc finger C2H2-type
- Zinc finger C2H2 superfamily
- Integrase zinc-binding domain
- Zinc finger, C2H2 type
- BTB/POZ domain
- C2H2-type zinc finger
- Integrase zinc binding domain
- Zinc finger and BTB domain-containing protein 11, BTB/POZ domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ZBTB11 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 ZBTB11 as an antibody target. Whether an autoantibody or antibody against ZBTB11 could matter depends on whether native ZBTB11 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZBTB11 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 ZBTB11 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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