Transcript: PEG13:1
Basic information
LNCipedia transcript ID: PEG13:1
LNCipedia gene ID: PEG13
Location (hg19): chr8:141104993-141109236
Strand: -
Class: intronic
Sequence Ontology term: sense_intronic_ncRNA
Transcript size: 4244 bp
Exons: 1
Sources: Ensembl release 83 - Dec 2015
Alternative transcript names: ENST00000631594.1
Alternative gene names: ENSG00000282164.1; PEG13;
RNA sequence:
Structure:
Protein coding potential
In stringent set: no
Locus conservation
Available literature
- Court (2014), Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment., Genome Res.
- Court (2014), The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus., Epigenetics Chromatin
- Sánchez Delgado (2014), Screening individuals with intellectual disability, autism and Tourette's syndrome for KCNK9 mutations and aberrant DNA methylation within the 8q24 imprinted cluster., Am. J. Med. Genet. B Neuropsychiatr. Genet.
LNCipedia transcript ID history
| LNCipedia version | LNCipedia transcript ID |
|---|---|
| 4.0 | PEG13:1 |
| 4.1 | PEG13:1 |
| 5.0 | PEG13:1 |
| 5.1 | PEG13:1 |
| 5.2 | PEG13:1 |