Details of Epigenetic Molecule(EM)
| General Information of EM (ID: EM03112) | |||||||
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| Official Symbol |
NR2F1-AS1
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| Official Full Name |
NR2F1 antisense RNA 1
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| Synonym |
FLJ42709
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| Molecule Type |
LncRNA
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| Position On Chromosome |
chr5(Start:93360779 - End:93585649)
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| Strand |
-
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| ENSG ID | |||||||
| NONCODE ID | |||||||
| Dnmivd Disease | |||||||
| Disease Relevance (Click to Show/Hide) | |||||||
| 8A40: Multiple sclerosis | Multiple sclerosis [Multiple sclerosis] | ||||||
| Detailed Information |
Disease Link
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| 8E49: Postviral fatigue syndrome | Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) [Postviral fatigue syndrome] | ||||||
| Detailed Information |
Disease Link
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| DD70: Crohn disease | Crohn's disease [Crohn disease] | ||||||
| Detailed Information |
Disease Link
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| XH1511: Ependymoma | Posterior fossa ependymoma [Ependymoma] | ||||||
| Detailed Information |
Disease Link
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| XH8P29: Medulloblastoma | Medulloblastoma [Medulloblastoma] | ||||||
| Detailed Information |
Disease Link
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| Protein(s) with this epigenetic modification | |||||||
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| Protein Name: Rv2966c | |||||||
| Detailed Information |
Pro Info
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[1] | |||||
| Description |
Rv2966c could hypermethylate the non-CpG dinucleotides at the host NR2F1-AS1 (intergenic) genetic loci during Mycobacterium tuberculosis H37Rv infection.
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| Protein Name: Rv2966c | |||||||
| Detailed Information |
Pro Info
click to show the detail information of this protein
|
[1] | |||||
| Description |
Rv2966c could hypermethylate the non-CpG dinucleotides at the host NR2F1-AS1 (geneBody) genetic loci during Mycobacterium tuberculosis H37Rv infection.
|
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| Protein Name: Rv2966c | |||||||
| Detailed Information |
Pro Info
click to show the detail information of this protein
|
[1] | |||||
| Description |
Rv2966c could hypomethylate the non-CpG dinucleotides at the host NR2F1-AS1 (intergenic) genetic loci during Mycobacterium tuberculosis H37Rv infection.
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| References | |||||
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| 1 | Genome-wide non-CpG methylation of the host genome during M. tuberculosis infection. Sci Rep. 2016 Apr 26;6:25006. doi: 10.1038/srep25006. | ||||
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