ZBTB22
Zinc finger and BTB domain-containing protein 22
Also known as: BING1, fru, fruitless, ZBT22_HUMAN, ZBTB22A, ZNF297, ZNF297A
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O15209
- Gene
- ZBTB22
- Ensembl
- ENSG00000236104
- Chromosome
- 6
- Canonical length
- 634 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
634 residues, UniProt reviewed canonical sequence.
>O15209|ZBTB22
1 MEPSPLSPSG AALPLPLSLA PPPLPLPAAA VVHVSFPEVT SALLESLNQQ RLQGQLCDVS
61 IRVQGREFRA HRAVLAASSP YFHDQVLLKG MTSISLPSVM DPGAFETVLA SAYTGRLSMA
121 AADIVNFLTV GSVLQMWHIV DKCTELLREG RASATTTITT AAATSVTVPG AGVPSGSGGT
181 VAPATMGSAR SHASSRASEN QSPSSSNYFS PRESTDFSSS SQEAFAASAV GSGERRGGGP
241 VFPAPVVGSG GATSGKLLLE ADELCDDGGD GRGAVVPGAG LRRPTYTPPS IMPQKHWVYV
301 KRGGNCPAPT PLVPQDPDLE EEEEEEDLVL TCEDDEDEEL GGSSRVPVGG GPEATLSISD
361 VRTLSEPPDK GEEQVNFCES SNDFGPYEGG GPVAGLDDSG GPTPSSYAPS HPPRPLLPLD
421 MQGNQILVFP SSSSSSSSQA PGQPPGNQAE HGAVTVGGTS VGSLGVPGSV GGVPGGTGSG
481 DGNKIFLCHC GKAFSHKSMR DRHVNMHLNL RPFDCPVCNK KFKMKHHLTE HMKTHTGLKP
541 YECGVCAKKF MWRDSFMRHR GHCERRHRLG GVGAVPGPGT PTGPSLPSKR ESPGVGGGSG
601 DEASAATPPS SRRVWSPPRV HKVEMGFGGG GGANLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZBTB22 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)
- 0.61
- Highest tissue expression
- 18 nTPM
Expression across tissuesHPA
Tissue
- skin: 18 nTPM
- cervix: 15 nTPM
- endometrium: 15 nTPM
- adrenal gland: 14 nTPM
- blood vessel: 14 nTPM
- cerebral cortex: 14 nTPM
Single-cell type
- ependymal cells: 9.5 nCPM
- bergmann glia: 5.4 nCPM
- papillary tip epithelial cells: 4.2 nCPM
- microglia: 3.8 nCPM
- other brain neurons: 3.8 nCPM
- oligodendrocyte progenitor cells: 3.6 nCPM
Immune cell
- basophil: 0.8 nTPM
- eosinophil: 0.8 nTPM
- naive CD4 T-cell: 0.7 nTPM
- memory B-cell: 0.5 nTPM
- memory CD4 T-cell: 0.4 nTPM
- plasmacytoid DC: 0.4 nTPM
Brain region
- cerebral cortex: 6.2 nTPM
- medulla oblongata: 4.8 nTPM
- spinal cord: 3.9 nTPM
- midbrain: 3.6 nTPM
- pons: 3.6 nTPM
- white matter: 3.6 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)
- 0.58
- gnomAD pLI
- 0.22
- gnomAD missense Z
- 1.86
- DepMap mean gene effect
- -0.05
- 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
- DNA-binding transcription factor activity, RNA polymerase II-specific
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- sequence-specific double-stranded DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZBTB22 as an antibody target. Whether an autoantibody or antibody against ZBTB22 could matter depends on whether native ZBTB22 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZBTB22 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 ZBTB22 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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