| Name | NLGN1 antisense RNA 1 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nAlthough the query requested a summary for the function of NLGN1‑AS1, none of the provided abstracts mention or investigate this transcript. Instead, the literature exclusively focuses on tissue transglutaminase (TG2) and its many roles in physiology and pathology. These studies demonstrate that TG2 is a multifunctional enzyme involved in diverse biological processes such as the clearance of apoptotic cells, activation of transforming growth factor‑β (TGF‑β), and modulation of inflammatory signaling pathways (e.g., NF‑κB, RhoA, and β‑catenin) that govern cell survival, adhesion, migration, and extracellular matrix stabilization."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "6"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nOther reports dissect TG2’s extracellular functions, showing that its interaction with matrix proteins (such as fibronectin) and cell surface receptors (including integrins and heparan sulfate proteoglycans) is critical for cell adhesion, migration, and tissue repair. Moreover, TG2’s regulated secretion and activity—modulated by redox conditions, post‐translational modifications, and interactions with partners such as thioredoxin—directly impact processes like fibrogenesis in the kidney, liver, and lung."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "7", "end_ref": "12"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAdditional investigations highlight TG2’s involvement in intracellular signaling and transcriptional regulation. For instance, TG2 can phosphorylate key substrates like the retinoblastoma protein (Rb), thereby influencing cell cycle progression, while its regulation of NF‑κB and β‑catenin pathways contributes to osteoblast differentiation, vascular calcification, and even cancer progression. TG2’s roles extend to mitochondrial homeostasis and autophagy, where its activity affects energy production and the clearance of damaged organelles."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "13", "end_ref": "18"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFurther studies elucidate how TG2 is integrated into networks controlling its own extracellular availability and activity. Its regulation via redox-dependent modifications (e.g., S‑nitrosylation), interactions with thioredoxin, and endocytosis through receptors such as low‑density lipoprotein receptor‑related protein 1 exemplify mechanisms by which cells fine‑tune TG2’s contributions to vascular stiffness, neurodegeneration, and tumor metastasis."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "19", "end_ref": "24"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFinally, emerging evidence extends TG2’s functional repertoire to the regulation of angiogenesis, neuronal survival, and tumor cell behavior via interactions with receptors like GPR56 and by modulating extracellular matrix deposition. Collectively, these findings underscore TG2 as a critical effector molecule in cellular homeostasis and disease pathogenesis."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "25", "end_ref": "30"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nRecent advances also illustrate TG2’s part in modulating tumor progression through its interactions with G protein–coupled receptors and its regulated internalization and degradation, further linking TG2 activity to alterations in extracellular matrix architecture and cell–matrix communication."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "31", "end_ref": "35"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn summary, while the original query aimed to elucidate the role of NLGN1‑AS1, the provided abstracts do not offer any insights into its function. Instead, they collectively illuminate the extensive and varied roles of TG2 in mediating apoptosis clearance, inflammation, tissue fibrosis, extracellular matrix remodeling, intracellular signaling, and other critical cellular processes. The biological functions and regulatory mechanisms of NLGN1‑AS1 remain unaddressed in these studies.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Zita Balklava, Elisabetta Verderio, Russell Collighan, et al. 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| NCBI Gene ID | 100874010 |
| API | |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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NLGN1-AS1 has 1 functional associations with biological entities spanning 1 categories (cell line, cell type or tissue) extracted from 1 datasets.
Click the + buttons to view associations for NLGN1-AS1 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of NLGN1-AS1 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. | |