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
In stringent set: yes
Locus conservation
Locus conservation? | ||||
---|---|---|---|---|
SMCR2:1 | no | no | no | no |
Available literature
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 |