Human Gene NDN (ENST00000331837.5) Description and Page Index
Description: Homo sapiens necdin, MAGE family member (NDN), mRNA. (from RefSeq NM_002487) RefSeq Summary (NM_002487): This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress growth in postmitotic neurons. [provided by RefSeq, Jul 2008]. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##RefSeq-Attributes-START## imprinted gene :: PMID: 9302265 ##RefSeq-Attributes-END## Gencode Transcript: ENST00000331837.5 Gencode Gene: ENSG00000182636.5 Transcript (Including UTRs) Position: hg38 chr15:23,685,400-23,687,330 Size: 1,931 Total Exon Count: 1 Strand: - Coding Region Position: hg38 chr15:23,686,252-23,687,217 Size: 966 Coding Exon Count: 1
The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
ModBase Predicted Comparative 3D Structure on X5D982
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Orthologous Genes in Other Species
Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.