ZNF774
Zinc finger protein 774
Also known as: MGC75360, ZN774_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6NX45
- Gene
- ZNF774
- Ensembl
- ENSG00000196391
- Chromosome
- 15
- Canonical length
- 483 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Intermediate filaments,Cytosol
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 transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
483 residues, UniProt reviewed canonical sequence.
>Q6NX45|ZNF774
1 MWLGTSGKSG LPGHCLENPL QECHPAQLEE WALKGISRPS VISQPEQKEE PWVLPLQNFE
61 ARKIPRESHT DCEHQVAKLN QDNSETAEQC GTSSERTNKD LSHTLSWGGN WEQGLELEGQ
121 HGTLPGEGQL ESFSQERDLN KLLDGYVGEK PMCAECGKSF NQSSYLIRHL RTHTGERPYT
181 CIECGKGFKQ SSDLVTHRRT HTGEKPYQCK GCEKKFSDSS TLIKHQRTHT GERPYECPEC
241 GKTFGRKPHL IMHQRTHTGE KPYACLECHK SFSRSSNFIT HQRTHTGVKP YRCNDCGESF
301 SQSSDLIKHQ RTHTGERPFK CPECGKGFRD SSHFVAHMST HSGERPFSCP DCHKSFSQSS
361 HLVTHQRTHT GERPFKCENC GKGFADSSAL IKHQRIHTGE RPYKCGECGK SFNQSSHFIT
421 HQRIHLGDRP YRCPECGKTF NQRSHFLTHQ RTHTGEKPFH CSKCNKSFRQ KAHLLCHQNT
481 HLILocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF774 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
- 6.7 nTPM
Expression across tissuesHPA
Tissue
- tongue: 6.7 nTPM
- rectum: 6.6 nTPM
- skeletal muscle: 5.7 nTPM
- seminal vesicle: 5.4 nTPM
- cerebellum: 4.8 nTPM
- cerebral cortex: 4.5 nTPM
Single-cell type
- myonuclei: 42 nCPM
- adrenal cortex cells: 23 nCPM
- early primary spermatocytes: 17 nCPM
- late spermatids: 17 nCPM
- late primary spermatocytes: 16 nCPM
- brain inhibitory neurons: 16 nCPM
Immune cell
- basophil: 1.3 nTPM
- neutrophil: 1.1 nTPM
- eosinophil: 0.7 nTPM
- NK-cell: 0.7 nTPM
- myeloid DC: 0.6 nTPM
- naive B-cell: 0.4 nTPM
Brain region
- cerebellum: 24 nTPM
- basal ganglia: 24 nTPM
- cerebral cortex: 22 nTPM
- white matter: 22 nTPM
- hypothalamus: 21 nTPM
- amygdala: 20 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)
- 1.48
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.17
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- selective
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 ZNF774 as an antibody target. Whether an autoantibody or antibody against ZNF774 could matter depends on whether native ZNF774 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF774 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 ZNF774 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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