ZNF211
Zinc finger protein 211
Also known as: CH2H2-25, ZN211_HUMAN, ZNF-25
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q13398
- Gene
- ZNF211
- Ensembl
- ENSG00000121417
- Chromosome
- 19
- Canonical length
- 564 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Mitochondria,Rods & Rings
OverviewNCBI Gene
This gene encodes a protein containing a Kruppel-associated box domain and multiple zinc finger domains. This protein may play a role in developmental processes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]
Canonical amino-acid sequenceUniProt
564 residues, UniProt reviewed canonical sequence.
>Q13398|ZNF211
1 MLGFPPGRPQ LPVQLRPQTR MATALRDPAS GSVTFEDVAV YFSWEEWDLL DEAQKHLYFD
61 VMLENFALTS SLGCWCGVEH EETPSEQRIS GERVPQFRTS KEGSSSQNAD SCEICCLVLR
121 DILHLAEHQG TNCGQKLHTC GKQFYISANL QQHQRQHITE APFRSYVDTA SFTQSCIVHV
181 SEKPFTCREI RKDFLANMRF LHQDATQTGE KPNNSNKCAV AFYSGKSHHN WGKCSKAFSH
241 IDTLVQDQRI LTREGLFECS KCGKACTRRC NLIQHQKVHS EERPYECNEC GKFFTYYSSF
301 IIHQRVHTGE RPYACPECGK SFSQIYSLNS HRKVHTGERP YECGECGKSF SQRSNLMQHR
361 RVHTGERPYE CSECGKSFSQ NFSLIYHQRV HTGERPHECN ECGKSFSRSS SLIHHRRLHT
421 GERPYECSKC GKSFKQSSSF SSHRKVHTGE RPYVCGECGK SFSHSSNLKN HQRVHTGERP
481 VECSECSKSF SCKSNLIKHL RVHTGERPYE CSECGKSFSQ SSSLIQHRRV HTGKRPYQCS
541 QCGKSFGCKS VLIQHQRVHI GEKPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF211 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
- 29 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 29 nTPM
- bone marrow: 22 nTPM
- cerebellum: 19 nTPM
- spleen: 17 nTPM
- retina: 17 nTPM
- pituitary gland: 17 nTPM
Single-cell type
- syncytiotrophoblasts: 31 nCPM
- bergmann glia: 30 nCPM
- retinal pigment epithelial cells: 26 nCPM
- astrocytes: 23 nCPM
- oligodendrocyte progenitor cells: 22 nCPM
- cardiomyocytes: 21 nCPM
Immune cell
- eosinophil: 12 nTPM
- MAIT T-cell: 12 nTPM
- naive CD4 T-cell: 12 nTPM
- T-reg: 12 nTPM
- memory CD8 T-cell: 11 nTPM
- naive B-cell: 11 nTPM
Brain region
- choroid plexus: 28 nTPM
- cerebellum: 19 nTPM
- amygdala: 17 nTPM
- white matter: 17 nTPM
- hypothalamus: 16 nTPM
- cerebral cortex: 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)
- 1.68
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.34
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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 ZNF211 as an antibody target. Whether an autoantibody or antibody against ZNF211 could matter depends on whether native ZNF211 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF211 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 ZNF211 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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