Details for Exon 19 of the Titin gene - Sequence Coordinates, Associated Transcripts, Functional Data, Truncating Variants and Sequence.
The genomic coordinates of HG19 and Locus Reference Genomic (LRG) and the CDS coordinates of the Titin meta-transcript for exon 19 are displayed below.
HG19 Genomic | HG38 Genomic | Locus Reference Genomic | Meta-Transcript | ||||
---|---|---|---|---|---|---|---|
Start | End | Start | End | Start | End | Start | End |
179,647,329 | 179,647,266 | 178,782,602 | 178,782,539 | 53,201 | 53,264 | 3,101 | 3,164 |
Exon 19 occurs in the following Titin transcripts (the number indicates the exon rank of exon 19 in each transcript).
META | N2BA | N2B | N2A | NOVEX-1 | NOVEX-2 | NOVEX-3 |
19 | 19 | 18 | 19 | 18 | 18 | 19 |
Region: This exon occurs in the near Z-disk region of the titin protein.
PSI: The "proportion spliced-in" (an estimate of the percentage of TTN transcripts that incorporate this exon based on RNAseq data) is 100% in DCM (LV tissue of 84 end-stage patients) and 100% in GTEx (LV tissue of 105 samples from Genotype-Tissue Expression project). (See Ref. 1 for details)
Symmetry: This exon is assymmetric, i.e. the length of the exon is not a multiple of three and therefore removal of it will alter the reading frame.
References
1. A. M. Roberts, J. S. Ware, D. S. Herman et al.
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease.
Sci. Transl. Med. 7, 270ra6 (2015).
The following TTN truncating variants affecting this exon have been described in major published studies (click on the study name for more details):
Study | Cohort | Patient ID | Variant (CDS) | Variant (protein) | Variant Type |
---|---|---|---|---|---|
NEJM 2012 | Controls | N-50 | c.3101-2A>T | essential splice site |
Size of Exon: 64 bases
Ensembl ID:
ENSE00002282639