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lncRNA Gene ID | lncRNA Symbol | mRNA Gene ID | mRNA Symbol | Possible gene function in psychiatric disorders |
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ENSMUST00000133808 | ENSMUSG00000087679 | ENSMUST00000129928 | Arhgef1 | Expressed in cortical neural progenitor cells to regulate neurite outgrowth |
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MERGE.17177.9 | MERGE.17177.9 | ENSMUST00000094280 | Chchd2 | Response to mitochondrial stress; its mutation is reported in patients with Parkinson’s disease |
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MERGE.19055.3 | MERGE.19055.3 | ENSMUST00000137133 | Fam107a | A unique link between stress and actin dynamics, which regulates long-term potentiation and cognition performance |
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MERGE.23389.1 | MERGE.23389.1 | ENSMUST00000064477 | Dlg1 | A known brake on myelination in the central nervous system |
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MERGE.26604.5 | MERGE.26604.5 | ENSMUST00000172835 | Nova2 | Encodes NOVA2, a neuron specific RNA-binding protein, which regulates axon guidance during cortical development |
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MERGE.32926.1 | MERGE.32926.1 | ENSMUST00000128145 | Dpf1 | Essential for post-mitotic neural development and dendritic morphogenesis |
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MERGE.36317.1 | MERGE.36317.1 | ENSMUST00000135214 | Shank3 | Encodes postsynaptic scaffolding protein SHANK3, essential for hyperpolarization activated cation channels, neuronal morphology, and synaptic connectivity |
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MERGE.41589.1 | ENSMUST00000135916 | MERGE.41589.1 | Dlg4 | Encodes postsynaptic density 95 (PSD95), a major synaptic protein that clusters glutamate receptors and is crucial for synaptic plasticity |
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NONMMUT035884.2 | NONMMUG022075.2 | ENSMUST00000129928 | Arhgef1 | Same as aforementioned |
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NONMMUT035884.2 | NONMMUG022075.2 | ENSMUST00000056129 | Npas4 | As immediate-early gene, Npas4 affects synaptic connection between excitatory and inhibitory neurons, neural circuit plasticity, and memory formation |
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NONMMUT045609.2 | NONMMUG028155.2 | ENSMUST00000135214 | Shank3 | Same as aforementioned |
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NONMMUT055012.2 | NONMMUG034136.2 | ENSMUST00000114317 | Grin1 | Encodes NMDA receptor GluN1 subunit; its mutation is reported in patients with epileptic encephalopathy, intellectual disability, and movement disorders |
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NONMMUT058932.2 | NONMMUG036638.2 | ENSMUST00000126866 | Sez6 | A candidate gene in autism, bipolar disorder, intellectual disability, and childhood onset schizophrenia |
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NONMMUT077752.1 | NONMMUG048253.1 | ENSMUST00000168513 | Pick1 | Encodes cytosolic protein PICK1, which facilitates the removal of GluA2 subunit from the synaptic plasma membrane |
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NONMMUT144756.1 | NONMMUG091158.1 | ENSMUST00000185503 | Dnajc13 | Dnajc13 mutation confers a toxic gain-of-function, impairs endosomal transport, and is an etiological contributor to Parkinson’s disease |
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NONMMUT149941.1 | NONMMUG094248.1 | ENSMUST00000020308 | Ddit4 | Encodes DDIT4, a negative regulator of myelination during peripheral nerve system development |
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