HomeAboutRankingsData Sources
© 2026 GeneE
🧬
GeneE
7 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
ⓘGeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
ZNF77
zinc finger protein 77
Chromosome 19 · 19p13.3
NCBI Gene: 58492Ensembl: ENSG00000175691.10HGNC: HGNC:13150UniProt: Q15935
19PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transcription Factor
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingnucleusDNA-binding transcription factor activity, RNA polymerase II-specificRNA polymerase II transcription regulatory region sequence-specific DNA bindingneurodegenerative diseasemyocardial infarctioncoronary artery diseaseIschemic stroke
✦AI Summary

ZNF77 (zinc finger protein 77) is a transcriptional regulator located on chromosome 19 that functions as a DNA-binding transcription factor for RNA polymerase II 1. The protein contains zinc finger motifs enabling sequence-specific DNA binding and nuclear localization for transcriptional regulation [GO annotations cited in provided data]. ZNF77 plays a critical role in controlling airway epithelial integrity and fungal susceptibility. The genetic variant rs35699176 (Q100*), a nonsense mutation causing premature truncation, disrupts bronchial epithelium integrity and increases extracellular matrix proteins, promoting Aspergillus fumigatus conidial adhesion and germination 2. Patients carrying this variant exhibit higher fungal loads in respiratory airways, suggesting ZNF77 as a key controller of Aspergillus colonization. ZNF77 mutations associate with multiple disease conditions. The Q100* variant links to elevated plasma IL-12 in fibromyalgia syndrome patients (11% prevalence) 3 and increased fasting growth hormone levels 4. ZNF77 variants also confer susceptibility to early-onset myocardial infarction and chr19 kidney disease 5, and hypo-HDL-cholesterolemia 6. Additionally, ZNF77 frameshift mutations in Meckel-Gruber syndrome fetuses suggest involvement in sonic hedgehog (SHH) signaling pathway regulation 7. Clinically, ZNF77 genotyping may inform genetic risk assessment for cardiovascular, renal, lipid, and fungal infection susceptibility.

Sources cited
1
ZNF77 chromosomal localization to 19p and confirmation of zinc finger motif cDNA characterization
PMID: 8478004
2
ZNF77 rs35699176 variant causes loss of bronchial epithelium integrity and promotes Aspergillus fumigatus colonization; associated with increased fungal loads in patients with fungal asthma
PMID: 30237437
3
ZNF77 Q100* nonsense mutation found in 11% of fibromyalgia syndrome patients with elevated IL-12 cytokine levels
PMID: 23762283
4
ZNF77 rs35699176 stop codon variant (MAF 4.8%) associated with increased fasting growth hormone concentration and height
PMID: 26086970
5
ZNF77 identified as novel locus conferring susceptibility to early-onset myocardial infarction and chronic kidney disease
PMID: 30226566
6
ZNF77 identified as novel locus for hypo-HDL-cholesterolemia susceptibility in early-onset dyslipidemia
PMID: 30365130
7
ZNF77 frameshift mutations in Meckel-Gruber syndrome fetuses; ZNF77 promotes CC2D2A expression and regulates sonic hedgehog (SHH) signaling
PMID: 34981460
Disease Associationsⓘ20
neurodegenerative diseaseOpen Targets
0.24Weak
myocardial infarctionOpen Targets
0.17Weak
coronary artery diseaseOpen Targets
0.17Weak
Ischemic strokeOpen Targets
0.17Weak
neoplasmOpen Targets
0.07Suggestive
chronic kidney diseaseOpen Targets
0.03Suggestive
hypertensionOpen Targets
0.02Suggestive
juvenile idiopathic arthritisOpen Targets
0.01Suggestive
retinal degenerationOpen Targets
0.01Suggestive
systemic juvenile idiopathic arthritisOpen Targets
0.01Suggestive
acute kidney injuryOpen Targets
0.01Suggestive
hypertrophic cardiomyopathyOpen Targets
0.01Suggestive
Autosomal dominant polycystic kidney diseaseOpen Targets
0.01Suggestive
cancerOpen Targets
0.01Suggestive
infectionOpen Targets
0.01Suggestive
Pleuropulmonary blastomaOpen Targets
0.01Suggestive
fibromyalgiaOpen Targets
0.01Suggestive
glioblastoma multiformeOpen Targets
0.01Suggestive
nonpapillary renal cell carcinomaOpen Targets
0.01Suggestive
colon carcinomaOpen Targets
0.01Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
P2RX3Protein interaction86%P2RX2Protein interaction86%MOB3CCo-mentioned in literature40%
Tissue Expression6 tissues
Bone Marrow
100%
Ovary
82%
Brain
64%
Lung
63%
Liver
61%
Heart
56%
Gene Interaction Network
Click a node to explore
ZNF77P2RX3P2RX2MOB3C
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt Q15935
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.65LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF1.08 [0.72–1.65]
RankingsWhere ZNF77 stands among ~20K protein-coding genes
  • #14,616of 20,598
    Most Researched19
  • #15,882of 17,882
    Most Constrained (LOEUF)1.65
Genes detectedZNF77
Sources retrieved7 papers
Response time—
📄 Sources
7▼
1
Identification of 13 novel susceptibility loci for early-onset myocardial infarction, hypertension, or chronic kidney disease.
PMID: 30226566
Int J Mol Med · 2018
1.00
2
Identification of 12 novel loci that confer susceptibility to early-onset dyslipidemia.
PMID: 30365130
Int J Mol Med · 2019
0.86
3
Chromosomal localization of four human zinc finger cDNAs.
PMID: 8478004
Hum Genet · 1993
0.71
4
Lung colonization by Aspergillus fumigatus is controlled by ZNF77.
PMID: 30237437
Nat Commun · 2018
0.57
5
Discovery of potential new gene variants and inflammatory cytokine associations with fibromyalgia syndrome by whole exome sequencing.
PMID: 23762283
PLoS One · 2013
0.43