ZNF695
Zinc finger protein 695
Also known as: SBZF3, ZN695_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IW36
- Gene
- ZNF695
- Ensembl
- ENSG00000197472
- Chromosome
- 1
- Canonical length
- 515 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nuclear speckles
OverviewNCBI Gene
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
515 residues, UniProt reviewed canonical sequence.
>Q8IW36|ZNF695
1 MGLLAFRDVA LEFSPEEWEC LDPAQRSLYR DVMLENYRNL ISLGEDSFNM QFLFHSLAMS
61 KPELIICLEA RKEPWNVNTE KTARHSVLSS YLTEDILPEQ GLQVSFQKVM LRRYERCCLE
121 KLRLRNDWEI VGEWKGQKAS YNGLDLCSAT THSKNFQCNK CVKGFSKFAN LNKCKISHTG
181 EKPFKCKECG NVSCMSLIMT QQQRIHIGEN PYQCKKCGKA FNECSCFTDC KRIHVGEKHC
241 KCEECNNIFK SCSSLAVVEK NHTEKKTYRC EECGKAFNLC SVLTKHKKIH TGEKPYKCEE
301 CGKSFKLFPY LTQHKRIHSR EKPYKCEECG KVFKLLSYLT QHRRIHTGEK TFRCEECGKA
361 FNQSSHLTEH RRIHTGEKPY KCEECGKAFT WFSYLIQHKR IHTGQKPYKC EECGKAFTWF
421 SYLTQHKRIH TGEKPYKCDE CGKAFNWFSY LTNHKRIHTG EKPYKCEECG KAFGQSSHLS
481 KHKTIHTREK PYKCEECGKA FNHSAQLAVH EKTHTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF695 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)
- 0.43
- Highest tissue expression
- 0.8 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 0.8 nTPM
- small intestine: 0.5 nTPM
- testis: 0.5 nTPM
- rectum: 0.4 nTPM
- breast: 0.3 nTPM
- pancreas: 0.3 nTPM
Single-cell type
- oocytes: 4.6 nCPM
- epididymal clear cells: 2 nCPM
- erythrocyte progenitors: 1.6 nCPM
- late primary spermatocytes: 1.1 nCPM
- kupffer cells: 1 nCPM
- megakaryocyte progenitors: 0.7 nCPM
Immune cell
- neutrophil: 0.7 nTPM
- basophil: 0.1 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebral cortex: 2.7 nTPM
- hippocampal formation: 2.6 nTPM
- white matter: 2.3 nTPM
- amygdala: 2.2 nTPM
- basal ganglia: 2 nTPM
- cerebellum: 2 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)
- 1.85
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.17
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% 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 ZNF695 as an antibody target. Whether an autoantibody or antibody against ZNF695 could matter depends on whether native ZNF695 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF695 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 ZNF695 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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