ZNF790
Zinc finger protein 790
Also known as: FLJ20350, MGC62100, ZN790_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6PG37
- Gene
- ZNF790
- Ensembl
- ENSG00000197863
- Chromosome
- 19
- Canonical length
- 636 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoli
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
636 residues, UniProt reviewed canonical sequence.
>Q6PG37|ZNF790
1 MAHLMMFRDV AVDFSQEEWE CLDLEQRDLY RDVMLENYSN MVSLGFCIYQ PEAFSLLEKG
61 KEPWKILRDE TRGPCPDMQS RCQTKKLLPK NGIFEREIAQ LEIMRICKNH SLDCLCFRGD
121 WEGNTQFQTL QDNQEECFKQ VIRTCEKRPT FNQHTVFNLH QRLNTGDKLN EFKELGKAFI
181 SGSDHTQHQL IHTSEKFCGD KECGNTFLPD SEVIQYQTVH TVKKTYECKE CGKSFSLRSS
241 LTGHKRIHTG EKPFKCKDCG KAFRFHSQLS VHKRIHTGEK SYECKECGKA FSCGSDLTRH
301 QRIHTGEKPY ECNECRKAFS QRSHLIKHQR IHTGEKPYEC KECGKAFTRG SHLTQHQRIH
361 TGEKSHECKE CGKAFIRGSN LAQHQNVHVG RKPYKCEKCG KAYIWSSHLA RHQRIHTGRK
421 PYECKQCGKT FTWASYLAQH EKIHNERKSY ECKECGKTFL HGSEFNRHQK IHTGERNYEC
481 KECGKTFFRG SELNRHQKIH TGKRPYECEE CGKAFLWGSQ LTRHQRMHTG EEPYVCKECG
541 KSFIWGSQLT RHKKIHTDAE PYGCKKSSHI FSHHSYFTEQ KIHNSANLCE WTDYGNTFSH
601 ESNFAQHQNI YTFEKSYEFK DFEKAFSSSS HFISLLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZNF790 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
- 10 nTPM
Expression across tissuesHPA
Tissue
- testis: 10 nTPM
- skin: 8.9 nTPM
- liver: 8.2 nTPM
- thyroid gland: 7.5 nTPM
- retina: 7.4 nTPM
- kidney: 5.5 nTPM
Single-cell type
- early spermatids: 185 nCPM
- cardiomyocytes: 100 nCPM
- retinal bipolar cells: 58 nCPM
- rod photoreceptor cells: 48 nCPM
- late spermatids: 47 nCPM
- fibro-adipogenic progenitors: 46 nCPM
Immune cell
- naive B-cell: 7.8 nTPM
- memory B-cell: 6.8 nTPM
- naive CD4 T-cell: 5.8 nTPM
- memory CD4 T-cell: 5.6 nTPM
- memory CD8 T-cell: 5.6 nTPM
- eosinophil: 5.1 nTPM
Brain region
- cerebellum: 31 nTPM
- medulla oblongata: 25 nTPM
- hypothalamus: 24 nTPM
- white matter: 24 nTPM
- midbrain: 22 nTPM
- basal ganglia: 22 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)
- 1.33
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.17
- DepMap mean gene effect
- 0.16
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% 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 ZNF790 as an antibody target. Whether an autoantibody or antibody against ZNF790 could matter depends on whether native ZNF790 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZNF790 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 ZNF790 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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