ZNF12
Zinc finger protein 12
Also known as: GIOT-3, KOX3, ZNF12_HUMAN, ZNF325
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P17014
- Gene
- ZNF12
- Ensembl
- ENSG00000164631
- Chromosome
- 7
- Canonical length
- 697 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Centrosome
OverviewNCBI Gene
This gene is a member of the krueppel C2H2-type zinc-finger protein family and encodes a protein with eight C2H2-type zinc fingers and a KRAB domain. This nuclear protein is involved in developmental control of gene expression. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
697 residues, UniProt reviewed canonical sequence.
>P17014|ZNF12
1 MNKSLGPVSF KDVAVDFTQE EWQQLDPEQK ITYRDVMLEN YSNLVSVGYH IIKPDVISKL
61 EQGEEPWIVE GEFLLQSYPD EVWQTDDLIE RIQEEENKPS RQTVFIETLI EERGNVPGKT
121 FDVETNPVPS RKIAYKNSLC DSCEKCLTSV SEYISSDGSY ARMKADECSG CGKSLLHIKL
181 EKTHPGDQAY EFNQNGEPYT LNEESLYQKI RILEKPFEYI ECQKAFQKDT VFVNHMEEKP
241 YKWNGSEIAF LQMSDLTVHQ TSHMEMKPYE CSECGKSFCK KSKFIIHQRT HTGEKPYECN
301 QCGKSFCQKG TLTVHQRTHT GEKPYECNEC GKNFYQKLHL IQHQRTHSGE KPYECSYCGK
361 SFCQKTHLTQ HQRTHSGERP YVCHDCGKTF SQKSALNDHQ KIHTGVKLYK CSECGKCFCR
421 KSTLTTHLRT HTGEKPYECN ECGKFFSRLS YLTVHYRTHS GEKPYECNEC GKTFYLNSAL
481 MRHQRVHTGE KPYECNECGK LFSQLSYLTI HHRTHSGVKP YECSECGKTF YQNSALCRHR
541 RIHKGEKPYE CYICGKFFSQ MSYLTIHHRI HSGEKPYECS ECGKTFCQNS ALNRHQRTHT
601 GEKAYECYEC GKCFSQMSYL TIHHRIHSGE KPFECNECGK AFSRMSYLTV HYRTHSGEKP
661 YECTECGKKF YHKSAFNSHQ RIHRRGNMNV IDVGRLLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF12 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)
- 0.46
- Highest tissue expression
- 17 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 17 nTPM
- retina: 14 nTPM
- epididymis: 13 nTPM
- thyroid gland: 13 nTPM
- endometrium: 13 nTPM
- ovary: 13 nTPM
Single-cell type
- esophageal apical cells: 46 nCPM
- gastric progenitor cells: 36 nCPM
- basal keratinocytes: 31 nCPM
- adrenal cortex cells: 31 nCPM
- corticotrophs: 30 nCPM
- pituicytes/fscs: 30 nCPM
Immune cell
- basophil: 8.7 nTPM
- MAIT T-cell: 1.9 nTPM
- naive CD8 T-cell: 1.9 nTPM
- memory CD8 T-cell: 1.6 nTPM
- naive CD4 T-cell: 1.5 nTPM
- gdT-cell: 1.4 nTPM
Brain region
- cerebellum: 26 nTPM
- choroid plexus: 22 nTPM
- thalamus: 21 nTPM
- pons: 20 nTPM
- midbrain: 20 nTPM
- amygdala: 19 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)
- 0.51
- gnomAD pLI
- 0.04
- gnomAD missense Z
- 1.49
- DepMap mean gene effect
- 0.02
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 13% 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
- sequence-specific double-stranded DNA binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZNF12 as an antibody target. Whether an autoantibody or antibody against ZNF12 could matter depends on whether native ZNF12 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF12 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 ZNF12 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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