ZNF264
Zinc finger protein 264
Also known as: KIAA0412, ZN264_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O43296
- Gene
- ZNF264
- Ensembl
- ENSG00000083844
- Chromosome
- 19
- Canonical length
- 627 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes a zinc finger protein and belongs to the krueppel C2H2-type zinc-finger protein family. Zinc finger proteins are often localized in the nucleus, bind nucleic acids, and regulate transcription. [provided by RefSeq, Jan 2010]
Canonical amino-acid sequenceUniProt
627 residues, UniProt reviewed canonical sequence.
>O43296|ZNF264
1 MAAAVLTDRA QVSVTFDDVA VTFTKEEWGQ LDLAQRTLYQ EVMLENCGLL VSLGCPVPKA
61 ELICHLEHGQ EPWTRKEDLS QDTCPGDKGK PKTTEPTTCE PALSEGISLQ GQVTQGNSVD
121 SQLGQAEDQD GLSEMQEGHF RPGIDPQEKS PGKMSPECDG LGTADGVCSR IGQEQVSPGD
181 RVRSHNSCES GKDPMIQEEE NNFKCSECGK VFNKKHLLAG HEKIHSGVKP YECTECGKTF
241 IKSTHLLQHH MIHTGERPYE CMECGKAFNR KSYLTQHQRI HSGEKPYKCN ECGKAFTHRS
301 NFVLHNRRHT GEKSFVCTEC GQVFRHRPGF LRHYVVHSGE NPYECLECGK VFKHRSYLMW
361 HQQTHTGEKP YECSECGKVF LESAALIHHY VIHTGEKPFE CLECGKAFNH RSYLKRHQRI
421 HTGEKPFVCS ECGKAFTHCS TFILHKRAHT GEKPFECKEC GKAFSNRKDL IRHFSIHTGE
481 KPYECVECGK AFTRMSGLTR HKRIHSGEKP YECVECGKSF CWSTNLIRHA IIHTGEKPYK
541 CSECGKAFSR SSSLTQHQRM HTGKNPISVT DVGRPFTSGQ TSVTLRELLL GKDFLNVTTE
601 ANILPEETSS SASDQPYQRE TPQVSSLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF264 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)
- 0.48
- Highest tissue expression
- 9.3 nTPM
Expression across tissuesHPA
Tissue
- testis: 9.3 nTPM
- retina: 8.1 nTPM
- bone marrow: 7.7 nTPM
- spleen: 7.7 nTPM
- pancreas: 7.4 nTPM
- thymus: 7.4 nTPM
Single-cell type
- adrenal medulla cells: 64 nCPM
- respiratory ciliated cells: 63 nCPM
- thyrotrophs: 48 nCPM
- fallopian tube ciliated cells: 47 nCPM
- somatotrophs: 44 nCPM
- endometrial ciliated cells: 44 nCPM
Immune cell
- eosinophil: 4.3 nTPM
- memory B-cell: 4.2 nTPM
- naive CD4 T-cell: 3.4 nTPM
- naive CD8 T-cell: 3.2 nTPM
- memory CD4 T-cell: 2.7 nTPM
- NK-cell: 2.4 nTPM
Brain region
- medulla oblongata: 46 nTPM
- white matter: 45 nTPM
- choroid plexus: 41 nTPM
- cerebellum: 38 nTPM
- thalamus: 36 nTPM
- basal ganglia: 35 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)
- 0.99
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.28
- DepMap mean gene effect
- 0.06
- 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
InteractionsUniProt · HPA
Protein binding partners of ZNF264 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 ZNF264 as an antibody target. Whether an autoantibody or antibody against ZNF264 could matter depends on whether native ZNF264 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF264 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 ZNF264 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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