Details for: ZNF117

Gene ID: 51351

Gene Type:  Protein-coding  - A gene that serves as a template for producing a messenger RNA (mRNA) molecule, which is then translated into a functional protein.

Symbol: ZNF117

Ensembl ID: ENSG00000152926

Description: zinc finger protein 117

Cell Significance Landscape

Associated with

  • Dna-binding transcription factor activity
    (GO:0003700)
  • Dna-binding transcription factor activity, rna polymerase ii-specific
    (GO:0000981)
  • Nucleus
    (GO:0005634)
  • Regulation of dna-templated transcription
    (GO:0006355)
  • Regulation of transcription by rna polymerase ii
    (GO:0006357)
  • Rna polymerase ii cis-regulatory region sequence-specific dna binding
    (GO:0000978)
  • Zinc ion binding
    (GO:0008270)

Significant Cells

Cell Significance Index (CSI) scores for the chosen context(s)

  • adipocyte CL0000136
    CSI 15.5
    rCSI 19.9%
    PRS 87.16
  • progenitor cell CL0011026
    CSI 8.44
    rCSI 17.95%
    PRS 88.19
  • fallopian tube secretory epithelial cell CL4030006
    CSI 4.4
    rCSI 4.23%
    PRS 92.59
  • epithelial cell of lower respiratory tract CL0002632
    CSI 3.59
    rCSI 2.78%
    PRS 95.55
  • neural crest cell CL0011012
    CSI 3.32
    rCSI 2.62%
    PRS 88.68
  • kidney loop of Henle thin ascending limb epithelial cell CL1001107
    CSI 3.2
    rCSI 8.28%
    PRS 92.09
  • peripheral nervous system neuron CL2000032
    CSI 3.18
    rCSI 4.34%
    PRS 88.64
  • interneuron CL0000099
    CSI 3.1
    rCSI 6.23%
    PRS 89.38
  • pro-B cell CL0000826
    CSI 2.86
    rCSI 2.36%
    PRS 94.54
  • hematopoietic precursor cell CL0008001
    CSI 2.84
    rCSI 2.92%
    PRS 97.15
  • epithelial cell of lung CL0000082
    CSI 2.73
    rCSI 2.27%
    PRS 94.78
  • differentiation-committed oligodendrocyte precursor CL4023059
    CSI 2.61
    rCSI 4.74%
    PRS 88.95
  • renal beta-intercalated cell CL0002201
    CSI 2.6
    rCSI 6.19%
    PRS 94.31
  • hepatic stellate cell CL0000632
    CSI 2.56
    rCSI 9.58%
    PRS 90.91
  • blood vessel endothelial cell CL0000071
    CSI 2.5
    rCSI 5.19%
    PRS 92.39
  • ciliated epithelial cell CL0000067
    CSI 2.46
    rCSI 2.16%
    PRS 86.77
  • kidney connecting tubule epithelial cell CL1000768
    CSI 2.39
    rCSI 6.05%
    PRS 89.82
  • kidney interstitial alternatively activated macrophage CL1000695
    CSI 2.37
    rCSI 6.17%
    PRS 95.22
  • epicardial adipocyte CL1000309
    CSI 2.28
    rCSI 7.4%
    PRS 91.52
  • alveolar adventitial fibroblast CL4028006
    CSI 2.21
    rCSI 3.48%
    PRS 94.65
  • CD14-low, CD16-positive monocyte CL0002396
    CSI 2.14
    rCSI 1.65%
    PRS 96.14
  • caudal ganglionic eminence derived cortical interneuron CL4023064
    CSI 2.14
    rCSI 3.78%
    PRS 83.66
  • endothelial cell of pericentral hepatic sinusoid CL0019022
    CSI 1.95
    rCSI 6%
    PRS 94.81
  • squamous epithelial cell CL0000076
    CSI 1.93
    rCSI 4.59%
    PRS 90.71
  • cerebral cortex GABAergic interneuron CL0010011
    CSI 1.93
    rCSI 5.7%
    PRS 93.39
  • astrocyte of the cerebral cortex CL0002605
    CSI 1.67
    rCSI 3.75%
    PRS 84.43
  • neural progenitor cell CL0011020
    CSI 1.21
    rCSI 5.33%
    PRS 84.72
  • megakaryocyte CL0000556
    CSI 1.12
    rCSI 4.88%
    PRS 93.97
  • retinal ganglion cell CL0000740
    CSI 0.91
    rCSI 2.02%
    PRS 85.74
  • GABAergic neuron CL0000617
    CSI 0.9
    rCSI 3.01%
    PRS 82.98
  • blood vessel smooth muscle cell CL0019018
    CSI 0.59
    rCSI 4.83%
    PRS 92.42

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this specific cell.

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.
Network Configuration

Explore relationships of the current gene. Select an Interaction Source: 'ONTOLOGY' for shared pathways (GO/Reactome) or 'STRING' for protein-protein interactions. Further refine by selecting context genes and comparing Cell Significance Index (CSI) scores between baseline and target cell types and their specific contexts.

Comma-separated if multiple.
Comma-separated if multiple.

Legend:
  • Query Gene
  • Node Color (Target Cell CSI, relative to current network):
    • Very High
    • High
    • Medium
    • Low
    • Very Low
    • CSI N/A
  • Node Size: Proportional to Target Cell CSI magnitude
  • STRING PPI Edge
  • Shared Pathway Edge (ONTOLOGY)

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Other Information

This section provides additional information about the gene, including a description generated by an AI language model and details about associated proteins.

## Summary [ZNF117](/details-gene/51351) is a protein-coding gene located on chromosome 7q11.21 that encodes for Zinc Finger Protein 117. Functional annotations strongly indicate its role as a DNA-binding transcription factor that operates within the nucleus to regulate transcription. Expression data highlights its particularly significant role in [adipocytes](/details-cell/CL0000136), where it shows an exceptionally high cell significance index. It also demonstrates notable expression across a wide range of cell types, including various [progenitor cells](/details-cell/CL0011026), epithelial cells, and neurons, suggesting a broad but context-specific regulatory function in cellular differentiation and maintenance. ## Cellular Roles and Expression Landscape The expression profile of [ZNF117](/details-gene/51351) reveals a diverse but distinct cellular landscape. **Overall**, its most significant expression is observed in [adipocytes](/details-cell/CL0000136) (CSI: 15.50), where its high significance suggests it may be a critical regulator of adipocyte identity or function. Beyond adipocytes, [ZNF117](/details-gene/51351) shows a recurring pattern of significance in various precursor and progenitor cell populations. This includes a high CSI in generalized [progenitor cells](/details-cell/CL0011026) (CSI: 8.44) as well as more specialized precursors such as [neural crest cells](/details-cell/CL0011012), [pro-B cells](/details-cell/CL0000826), [hematopoietic precursor cells](/details-cell/CL0008001), and [differentiation-committed oligodendrocyte precursors](/details-cell/CL4023059). This consistent association with developmental intermediates suggests a potential role in maintaining stemness or guiding early lineage commitment across multiple developmental axes. The gene is also significantly expressed in several specialized epithelial and endothelial cell types. These include [fallopian tube secretory epithelial cells](/details-cell/CL4030006), [epithelial cells of the lower respiratory tract](/details-cell/CL0002632), [kidney loop of Henle thin ascending limb epithelial cells](/details-cell/CL1001107), and [blood vessel endothelial cells](/details-cell/CL0000071). This broad expression pattern points to a fundamental role in regulating transcriptional programs that are essential for the function of diverse differentiated cell types. ## Pathways and Molecular Function Consistent with its identity as a zinc finger protein, the molecular functions of [ZNF117](/details-gene/51351) are centered on transcriptional regulation. Gene Ontology annotations confirm that it is located in the [nucleus](/details-cell/GO:0005634) and possesses [dna-binding transcription factor activity](/details-cell/GO:0003700), specifically binding to cis-regulatory regions to control transcription by RNA polymerase II ([GO:0000978](https://www.ebi.ac.uk/QuickGO/term/GO:0000978), [GO:0006357](https://www.ebi.ac.uk/QuickGO/term/GO:0006357)). It is also involved in the broader biological process of [regulation of dna-templated transcription](/details-cell/GO:0006355). Its function is dependent on [zinc ion binding](/details-cell/GO:0008270), which is characteristic of the C2H2-type zinc finger domains it contains. This molecular machinery allows [ZNF117](/details-gene/51351) to act as a regulator, likely orchestrating the specific gene expression programs required for the diverse cell types in which it is prominently expressed, such as adipocytes and various progenitor cells. ## Research Directions The available data points to [ZNF117](/details-gene/51351) as a key transcriptional regulator with highly specific cellular roles, particularly in adipocytes and progenitor cells. This provides a foundation for several testable hypotheses. **Proposed Hypotheses:** 1. Given its exceptionally high CSI in [adipocytes](/details-cell/CL0000136), [ZNF117](/details-gene/51351) is a master regulator of adipogenesis, controlling the terminal differentiation of pre-adipocytes into mature, lipid-storing adipocytes. 2. The consistent expression of [ZNF117](/details-gene/51351) across multiple, distinct progenitor populations ([hematopoietic](/details-cell/CL0008001), [neural](/details-cell/CL4023059), etc.) suggests it functions as a general gatekeeper of differentiation, maintaining cells in an undifferentiated state or controlling the initial steps of lineage commitment. **Experimental Approach:** To test the hypothesis that [ZNF117](/details-gene/51351) is a master regulator of adipogenesis (Hypothesis 1), a loss-of-function study could be performed. Human mesenchymal stem cells (MSCs) or pre-adipocyte cell lines could be transduced with a CRISPR-Cas9 system to knock out [ZNF117](/details-gene/51351). Control and knockout cells would then be subjected to a standard adipogenic differentiation cocktail. The impact of the knockout could be assessed by measuring key endpoints such as: - **Transcriptomic analysis (RNA-seq):** To identify changes in the expression of key adipogenic transcription factors (e.g., *PPARG*, *CEBPA*) and markers of mature adipocytes. - **Functional assays:** Quantifying lipid accumulation using Oil Red O staining and measuring the secretion of adipokines like adiponectin and leptin via ELISA. A failure of knockout cells to differentiate or a significantly impaired adipogenic phenotype would provide strong evidence for its critical role in this process. **Therapeutic Potential:** As a nuclear DNA-binding transcription factor, [ZNF117](/details-gene/51351) is a challenging direct target for small-molecule inhibitors. However, if it is validated as a key driver of adipogenesis, it could represent an important node in the regulatory network of metabolic health and disease. In conditions like obesity and type 2 diabetes, where excess or dysfunctional adipose tissue is a key pathological feature, modulating the activity of [ZNF117](/details-gene/51351) or its downstream targets could be a viable therapeutic strategy. Inhibition, rather than activation, would likely be the goal to limit the formation or expansion of adipose tissue.