ZNF721
Zinc finger protein 721
Also known as: KIAA1982, ZN721_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TF20
- Gene
- ZNF721
- Ensembl
- ENSG00000182903
- Chromosome
- 4
- Canonical length
- 911 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Centriolar satellite,Cytosol
OverviewNCBI Gene
Predicted to enable DNA binding activity and zinc ion 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
911 residues, UniProt reviewed canonical sequence.
>Q8TF20|ZNF721
1 MCSHFTQDFL PVQGIEDSFH KLILRRYEKC GHDNLQLRKG CKSMNVCKVQ KGVYNGINKC
61 LSNTQSKIFQ CNARVKVFSK FANSNKDKTR HTGEKHFKCN ECGKSFQKFS DLTQHKGIHA
121 GEKPYTCEER GKDFGWYTDL NQHKKIHTGE KPYKCEECGK AFNRSTNLTA HKRIHNREKA
181 YTGEDRDRAF GWSTNLNEYK KIHTGDKPYK CKECGKAFMH SSHLNKHEKI HTGEKPYKCK
241 ECGKVISSSS SFAKHKRIHT GEKPFKCLEC GKAFNISTTL TKHRRIHTGE KPYTCEVCGK
301 AFRQSANLYV HRRIHTGEKP YTCGECGKTF RQSANLYVHR RIHTGEKPYK CEDCGKAFGR
361 YTALNQHKKI HTGEKPYKCE ECGKAFNSST NLTAHKRIHT REKPYTCEDR GRAFGLSTNL
421 NEYKKIHTGD KPYKCKECGK AFIHSLHLNK HEKIHTGKKP YKCKQCGKVI TSSSSFAKHK
481 RIHTGEKPFE CLECGKAFTS STTLTKHRRI HTGEKPYTCE VCGKAFRQSA ILYVHRRIHT
541 GEKPYTCEEC GKTFRQSANL YVHRRIHTGE KPYKCEECGK AFGRYTDLNQ HKKIHTGEKL
601 YKCEECGKDF VWYTDLNQQK KIYTGEKPYK CEECGKAFAP STDLNQHTKI LTGEQSYKCE
661 ECGKAFGWSI ALNQHKKIHT GEKPYKCEEC GKAFSRSRNL TTHRRVHTRE KPYKCEDRGR
721 SFGWSTNLNE YKKIHTGDKL YKCKECGKVF KQSSHLNRHE KIHTGKKPYK CKECGKVITS
781 SSSFAKHKRI HTGEKPFKCL ECGKAFTSST TLTKHRRIHT GEKPYTCEEC GKAFRQSAIL
841 YVHRRIHTGE KPYTCGECGK TFRQSANLYA HKKIHTGEKP YTCGDCGKTF RQSANLYAHK
901 KIHTGDKTIQ VLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF721 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)
- 0.42
- Highest tissue expression
- 21 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 21 nTPM
- tonsil: 21 nTPM
- cerebellum: 19 nTPM
- retina: 18 nTPM
- thymus: 18 nTPM
- breast: 18 nTPM
Single-cell type
- distal convoluted tubule cells: 233 nCPM
- podocytes: 205 nCPM
- proximal tubule cells: 204 nCPM
- renal collecting duct intercalated cells: 201 nCPM
- renal connecting tubule cells: 187 nCPM
- loop of henle epithelial cells: 179 nCPM
Immune cell
- naive CD4 T-cell: 21 nTPM
- memory B-cell: 17 nTPM
- T-reg: 17 nTPM
- naive CD8 T-cell: 17 nTPM
- naive B-cell: 16 nTPM
- NK-cell: 14 nTPM
Brain region
- cerebellum: 64 nTPM
- cerebral cortex: 51 nTPM
- white matter: 49 nTPM
- hypothalamus: 43 nTPM
- basal ganglia: 43 nTPM
- amygdala: 42 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)
- 1.89
- gnomAD pLI
- 0.09
- gnomAD missense Z
- -1.77
- DepMap mean gene effect
- 0.22
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZNF721 as an antibody target. Whether an autoantibody or antibody against ZNF721 could matter depends on whether native ZNF721 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF721 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 ZNF721 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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