Transcript: SMCR2:1

Basic information

LNCipedia transcript ID: SMCR2:1 
HGNC Gene Symbol: SMCR2    
HGNC Full Gene Name: Smith-Magenis syndrome chromosome region, candidate 2
Ensembl Gene ID: ENSG00000223979
Ensembl Transcript ID: ENST00000456090
RefSeq ID: NR_131243
Location (hg38): chr17:17674026-17677688
Strand: -
Class: intergenic
Sequence Ontology term: lincRNA
Transcript size: 564 bp
Exons: 4
Sources: Broad Institute; Ensembl release 64 - Sep 2011; Gencode v13; Ensembl release 68 - Jul 2012; NONCODE v4; Ensembl release 75 - Feb 2014; Ensembl release 83 - Dec 2015; Ensembl release 87 - Dec 2016; Ensembl release 90 - Aug 2017; Ensembl release 92 - Apr 2018; Refseq - NCBI Annotation Release 106
Alternative transcript names: TCONS_00025215; ENST00000456090; ENST00000456090.2; SMCR2-001; OTTHUMT00000131667.2; NONHSAT146099; NR_131243.1
Alternative gene names: XLOC_012408; linc-PEMT; ENSG00000223979; SMCR2; ENSG00000223979.2; OTTHUMG00000059291.2;


RNA sequence:

Structure:

Protein coding potential

Metric Raw result Interpretation
PRIDE reprocessing 2.0 0 non-coding 
Lee translation initiation sites 0 non-coding 
PhyloCSF score -27.1889 non-coding 
CPAT coding probability 3.82% non-coding 
Bazzini small ORFs 0 non-coding 

In stringent set: yes

Locus conservation

Locus conservation?
SMCR2:1 no no no no

Available literature

  1. Bi (2002), Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse., Genome Res.


LNCipedia transcript ID history

LNCipedia version LNCipedia transcript ID
1.3 lnc-PEMT-1:1
3.1 lnc-PEMT-1:1
4.0 SMCR2:1
4.1 SMCR2:1
5.0 SMCR2:1
5.1 SMCR2:1
5.2 SMCR2:1