RNF213-AS1 Gene

Name RNF213 antisense RNA 1
Summary
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As such, no information regarding the cellular function, regulatory mechanisms, or physiological significance of RNF213‑AS1 can be extracted from this body of literature. The absence of any reference to RNF213‑AS1 highlights a gap in these studies relative to the extensive work on KCC isoforms and underscores the need for dedicated research to elucidate the potential roles of RNF213‑AS1.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Kerstin Piechotta, Jianming Lu, Eric Delpire "}, {"type": "b", "children": [{"type": "t", "text": "Cation chloride cotransporters interact with the stress-related kinases Ste20-related proline-alanine-rich kinase (SPAK) and oxidative stress response 1 (OSR1)."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M208108200"}], "href": "https://doi.org/10.1074/jbc.M208108200"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12386165"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12386165"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Heidi C Howard, David B Mount, Daniel Rochefort, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Nat Genet (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/ng1002"}], "href": "https://doi.org/10.1038/ng1002"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12368912"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12368912"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Thomas Boettger, Marco B Rust, Hannes Maier, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Loss of K-Cl co-transporter KCC3 causes deafness, neurodegeneration and reduced seizure threshold."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "EMBO J (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/emboj/cdg519"}], "href": "https://doi.org/10.1093/emboj/cdg519"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "14532115"}], "href": "https://pubmed.ncbi.nlm.nih.gov/14532115"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Kristopher T Kahle, Bianca Flores, Diana Bharucha-Goebel, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Peripheral motor neuropathy is associated with defective kinase regulation of the KCC3 cotransporter."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Signal (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1126/scisignal.aae0546"}], "href": "https://doi.org/10.1126/scisignal.aae0546"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27485015"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27485015"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Zhengsheng Li, Megan K Mulligan, Xusheng Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A transposon in Comt generates mRNA variants and causes widespread expression and behavioral differences among mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0012181"}], "href": "https://doi.org/10.1371/journal.pone.0012181"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20808911"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20808911"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Zesergio Melo, Silvia Cruz-Rangel, Rocio Bautista, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Molecular evidence for a role for K(+)-Cl(-) cotransporters in the kidney."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Physiol Renal Physiol (2013)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1152/ajprenal.00390.2013"}], "href": "https://doi.org/10.1152/ajprenal.00390.2013"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24089410"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24089410"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Dao Pan, Theodosia A Kalfa, Daren Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "K-Cl cotransporter gene expression during human and murine erythroid differentiation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M110.206516"}], "href": "https://doi.org/10.1074/jbc.M110.206516"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21733850"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21733850"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Jinlong Ding, Eric Delpire "}, {"type": "b", "children": [{"type": "t", "text": "Deletion of KCC3 in parvalbumin neurons leads to locomotor deficit in a conditional mouse model of peripheral neuropathy associated with agenesis of the corpus callosum."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Behav Brain Res (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbr.2014.08.005"}], "href": "https://doi.org/10.1016/j.bbr.2014.08.005"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25116249"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25116249"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Yuan-Ting Sun, Chi-Chang Shieh, Eric Delpire, et al. "}, {"type": "b", "children": [{"type": "t", "text": "K⁺-Cl⁻ cotransport mediates the bactericidal activity of neutrophils by regulating NADPH oxidase activation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Physiol (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1113/jphysiol.2011.225300"}], "href": "https://doi.org/10.1113/jphysiol.2011.225300"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22526882"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22526882"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Yuan-Ting Sun, Thy-Sheng Lin, Shun-Fen Tzeng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Deficiency of electroneutral K+-Cl- cotransporter 3 causes a disruption in impulse propagation along peripheral nerves."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Glia (2010)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/glia.21028"}], "href": "https://doi.org/10.1002/glia.21028"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "20549748"}], "href": "https://pubmed.ncbi.nlm.nih.gov/20549748"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Olivier Lucas, Cécile Hilaire, Eric Delpire, et al. "}, {"type": "b", "children": [{"type": "t", "text": "KCC3-dependent chloride extrusion in adult sensory neurons."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Neurosci (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.mcn.2012.05.005"}], "href": "https://doi.org/10.1016/j.mcn.2012.05.005"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22609694"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22609694"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Masoud Shekarabi, Adèle Salin-Cantegrel, Janet Laganière, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "A deletion mutation in Slc12a6 is associated with neuromuscular disease in gaxp mice."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Genomics (2008)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ygeno.2007.12.010"}], "href": "https://doi.org/10.1016/j.ygeno.2007.12.010"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "18343091"}], "href": "https://pubmed.ncbi.nlm.nih.gov/18343091"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "Melissa Bowerman, Céline Salsac, Véronique Bernard, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Genetic disruption of KCC cotransporters in a mouse model of thalassemia intermedia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Blood Cells Mol Dis (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bcmd.2019.102389"}], "href": "https://doi.org/10.1016/j.bcmd.2019.102389"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31835175"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31835175"}]}, {"type": "r", "ref": 18, "children": [{"type": "t", "text": "Bianca Flores, Eric Delpire "}, {"type": "b", "children": [{"type": "t", "text": "Osmotic Response of Dorsal Root Ganglion Neurons Expressing Wild-Type and Mutant KCC3 Transporters."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Physiol Biochem (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.33594/000000241"}], "href": "https://doi.org/10.33594/000000241"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32506846"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32506846"}]}, {"type": "r", "ref": 19, "children": [{"type": "t", "text": "Yuan-Ting Sun, Shun-Fen Tzeng, Thy-Sheng Lin, et al. "}, {"type": "b", "children": [{"type": "t", "text": "KCC3 deficiency-induced disruption of paranodal loops and impairment of axonal excitability in the peripheral nervous system."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neuroscience (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.neuroscience.2016.08.031"}], "href": "https://doi.org/10.1016/j.neuroscience.2016.08.031"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27568057"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27568057"}]}, {"type": "r", "ref": 20, "children": [{"type": "t", "text": "Boris E Shmukler, Alicia Rivera, Katherine Nishimura, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Erythroid-specific inactivation of Slc12a6/Kcc3 by EpoR promoter-driven Cre expression reduces K-Cl cotransport activity in mouse erythrocytes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Physiol Rep (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.14814/phy2.15186"}], "href": "https://doi.org/10.14814/phy2.15186"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35274823"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35274823"}]}, {"type": "r", "ref": 21, "children": [{"type": "t", "text": "Bianca Flores, Eric Delpire "}, {"type": "b", "children": [{"type": "t", "text": "Temporal manipulation of KCC3 expression in juvenile or adult mice suggests irreversible developmental deficit in hereditary motor sensory neuropathy with agenesis of the corpus callosum."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Physiol Cell Physiol (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1152/ajpcell.00594.2020"}], "href": "https://doi.org/10.1152/ajpcell.00594.2020"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33596149"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33596149"}]}]}]}
NCBI Gene ID 100294362
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Predicted Functions View RNF213-AS1's ARCHS4 Predicted Functions.
Co-expressed Genes View RNF213-AS1's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View RNF213-AS1's ARCHS4 Predicted Functions.

Functional Associations

RNF213-AS1 has 3 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 RNF213-AS1 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
GTEx Tissue-Specific Aging Signatures tissue samples with high or low expression of RNF213-AS1 gene relative to other tissue samples from the GTEx Tissue-Specific Aging Signatures dataset.