CCDC192 Gene

Name coiled-coil domain containing 192
Summary
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nThe study investigated MYCN amplification in neuroblastoma and identified that the RNF121 wild‐type protein plays an essential oncogenic role by localizing predominantly to the cis‐Golgi complex and directly interacting with MYCN, thereby enhancing its stability. A point mutation in RNF121 (M158R), which disrupts Golgi localization and reduces protein stability, resulted in a pronounced decrease in tumorigenicity in MYCN‐amplified neuroblastoma models. This work underlines the importance of RNF121 as a cofactor that amplifies MYCN-driven oncogenic signaling, with its expression levels serving as a predictive marker for poor prognosis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}, {"type": "p", "children": [{"type": "t", "text": "\nFurther findings revealed that the RNF121-enhanced growth of neuroblastoma cells is particularly reliant on its transmembrane Helix 5, emphasizing the structural elements of RNF121 crucial for its role in stabilizing MYCN. The clinical relevance is highlighted by the association between high RNF121 expression and poor outcomes not only in neuroblastoma but also in other MYC-driven malignancies, thereby positioning RNF121 as a potential target for drug development."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}, {"type": "p", "children": [{"type": "t", "text": "\nIt should be noted that although the abstract provides extensive details on the function of RNF121 as an oncogenic cofactor in MYCN amplification, there is no mention or data regarding CCDC192. Consequently, no functional role for CCDC192 can be inferred from the present study."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}]}]}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Belamy B Cheung, Ritu Mittra, Jayne Murray, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Golgi-localized Ring Finger Protein 121 is necessary for MYCN-driven neuroblastoma tumorigenesis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Commun Biol (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s42003-024-06899-8"}], "href": "https://doi.org/10.1038/s42003-024-06899-8"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "39402275"}], "href": "https://pubmed.ncbi.nlm.nih.gov/39402275"}]}]}]}
NCBI Gene ID 728586
API
Download Associations
Predicted Functions View CCDC192's ARCHS4 Predicted Functions.
Co-expressed Genes View CCDC192's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View CCDC192's ARCHS4 Predicted Functions.

Functional Associations

CCDC192 has 481 functional associations with biological entities spanning 6 categories (functional term, phrase or reference, disease, phenotype or trait, chemical, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 15 datasets.

Click the + buttons to view associations for CCDC192 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles tissue samples with high or low expression of CCDC192 gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset.
CM4AI KOLF21J CRISPRi Gene Perturbation Atlas gene perturbations changing expression of CCDC192 gene from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas dataset.
COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 cellular components co-occuring with CCDC192 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
DISEASES Experimental Gene-Disease Association Evidence Scores 2025 diseases associated with CCDC192 gene in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 diseases co-occuring with CCDC192 gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
GTEx eQTL 2025 SNPs regulating expression of CCDC192 gene from the GTEx eQTL 2025 dataset.
GTEx Tissue-Specific Aging Signatures tissue samples with high or low expression of CCDC192 gene relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset.
GWAS Catalog SNP-Phenotype Associations 2025 phenotypes associated with CCDC192 gene in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
JASPAR Predicted Human Transcription Factor Targets 2025 transcription factors regulating expression of CCDC192 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Human Transcription Factor Targets dataset.
JASPAR Predicted Mouse Transcription Factor Targets 2025 transcription factors regulating expression of CCDC192 gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Mouse Transcription Factor Targets 2025 dataset.
Rummagene Transcription Factor Associations 2026 transcription factors regulating expression of CCDC192 gene from the Rummagene Transcription Factor Associations 2026 dataset.
RummaGEO Drug Perturbation Signatures drug perturbations changing expression of CCDC192 gene from the RummaGEO Drug Perturbation Signatures dataset.
RummaGEO Gene Perturbation Signatures gene perturbations changing expression of CCDC192 gene from the RummaGEO Gene Perturbation Signatures dataset.
Sci-Plex Drug Perturbation Signatures drug perturbations changing expression of CCDC192 gene from the Sci-Plex Drug Perturbation Signatures dataset.
TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 tissues co-occuring with CCDC192 protein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.