| Name | TBC1D8 antisense RNA 1 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nAlthough none of the provided abstracts mention TBC1D8‐AS1, they collectively offer deep insights into the function of the homeobox transcription factor Barx1 in foregut and digestive tract development. In early gut organogenesis, Barx1 expression in mesenchymal cells is essential for directing overlying endodermal cells to adopt a stomach-specific epithelial fate rather than an intestinal one. This is achieved primarily through its induction of secreted Wnt antagonists that efficiently down‐regulate canonical Wnt signaling, thereby enabling proper stomach differentiation."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "3"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBarx1’s role extends beyond stomach epithelial specification. It is also integral to proper foregut patterning, including the processes of tracheo‐esophageal septation and the establishment of left–right asymmetry, as misexpression or loss of Barx1 results in homeotic transformations and malformations such as intestinal truncation, malrotation, and improper respiratory versus digestive identity. Moreover, aberrant Barx1 expression impacts the development of neighboring organs like the spleen, highlighting its wider role in coordinating mesenchymal–epithelial interactions during organogenesis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn addition, fine-tuning of Barx1 expression is achieved by post-transcriptional mechanisms involving miRNAs, such as miR-7a and miR-203, which down-regulate Barx1 levels at critical developmental stages to ensure proper stomach and intestinal morphogenesis. Further regulatory complexity is added by transcription factors like Hoxa2, which not only modulate Barx1 but also influence other downstream targets implicated in craniofacial and palatal development. Collectively, these studies underscore a multifaceted regulatory network in which suppression of Wnt signaling, tight spatio-temporal control of transcription factor expression, and miRNA-mediated modulation converge to shape digestive tract development."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Byeong-Moo Kim, Georg Buchner, Isabelle Miletich, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The stomach mesenchymal transcription factor Barx1 specifies gastric epithelial identity through inhibition of transient Wnt signaling."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Dev Cell (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.devcel.2005.01.015"}], "href": "https://doi.org/10.1016/j.devcel.2005.01.015"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15809042"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15809042"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Janghee Woo, Isabelle Miletich, Byeong-Moo Kim, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Barx1-mediated inhibition of Wnt signaling in the mouse thoracic foregut controls tracheo-esophageal septation and epithelial differentiation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0022493"}], "href": "https://doi.org/10.1371/journal.pone.0022493"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21799872"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21799872"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Byeong-Moo Kim, Isabelle Miletich, Junhao Mao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Independent functions and mechanisms for homeobox gene Barx1 in patterning mouse stomach and spleen."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Development (2007)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1242/dev.009308"}], "href": "https://doi.org/10.1242/dev.009308"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "17855428"}], "href": "https://pubmed.ncbi.nlm.nih.gov/17855428"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Chenura D Jayewickreme, Ramesh A Shivdasani "}, {"type": "b", "children": [{"type": "t", "text": "Control of stomach smooth muscle development and intestinal rotation by transcription factor BARX1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Dev Biol (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ydbio.2015.05.024"}], "href": "https://doi.org/10.1016/j.ydbio.2015.05.024"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26057579"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26057579"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Byeong-Moo Kim, Janghee Woo, Chryssa Kanellopoulou, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Regulation of mouse stomach development and Barx1 expression by specific microRNAs."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Development (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1242/dev.056317"}], "href": "https://doi.org/10.1242/dev.056317"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21307095"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21307095"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Tara M Smith, Xia Wang, Wei Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Hoxa2 plays a direct role in murine palate development."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Dev Dyn (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/dvdy.22040"}], "href": "https://doi.org/10.1002/dvdy.22040"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19653318"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19653318"}]}]}]}
|
| NCBI Gene ID | 100506286 |
| API | |
| Download Associations | |
| Predicted Functions |
![]() |
| Co-expressed Genes |
![]() |
| Expression in Tissues and Cell Lines |
![]() |
TBC1D8-AS1 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
Click the + buttons to view associations for TBC1D8-AS1 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary |
|---|