Special

HsaINT0169741 @ hg38

Intron Retention

Gene
ENSG00000166682 | TMPRSS5
Description
transmembrane protease, serine 5 [Source:HGNC Symbol;Acc:HGNC:14908]
Coordinates
chr11:113696858-113697418:-
Coord C1 exon
chr11:113697283-113697418
Coord A exon
chr11:113696972-113697282
Coord C2 exon
chr11:113696858-113696971
Length
311 bp
Sequences
Splice sites
5' ss Seq
CAGGTAACA
5' ss Score
8.88
3' ss Seq
TATTCCCTTCTTCTGCCAAGACT
3' ss Score
1.86
Exon sequences
Seq C1 exon
TATCTTTCAGAATAAACAGCGAAGACTTCTTGCTGGAAGCGCAAGTGAGGGATCAGCCACGCTGGCTCCTGGTCTGCCATGAGGGCTGGAGCCCCGCCCTGGGGCTGCAGATCTGCTGGAGCCTTGGGCATCTCAG
Seq A exon
GTAACAGGAGTTAGATGTGGGTCCTGTGAAGGGGGAGGCCTGGCTGGTGTGGGATGGGAATTGGAGACCTCTACCTGCCCGTCACTGGTCAATGTGCTCAGGAAATGTCAAGAGGTCTTTTTGGCCATCTTCTGGCCTCTGGGCACAATGGTGCCCCAGCCCATTTCTCTGTTTGGAGTATTACTGCTTTTTAACAAGCATAAACCCCAGCAGTAATCATTATCACAGTCTTGCGGTCACTATACTAGTATTATATCTCGTACATATTCCAGTTATGATTTCCTCCTGTTCTATTCCCTTCTTCTGCCAAG
Seq C2 exon
ACTCACTCACCACAAGGGAGTAAACCTCACTGACATCAAACTCAACAGTTCCCAGGAGTTTGCTCAGCTCTCTCCTAGACTGGGAGGCTTCCTGGAGGAGGCGTGGCAGCCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000166682:ENST00000299882:5
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF154941=SRCR_2=PU(39.8=84.8)
A:
NA
C2:
PF154941=SRCR_2=FE(38.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CAGAATAAACAGCGAAGACTTCTTGC
R:
CTGCCACGCCTCCTCCAG
Band lengths:
238-549
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains