HsaINT0169736 @ hg38
Intron Retention
Gene
ENSG00000166682 | TMPRSS5
Description
transmembrane protease, serine 5 [Source:HGNC Symbol;Acc:HGNC:14908]
Coordinates
chr11:113689765-113690373:-
Coord C1 exon
chr11:113690231-113690373
Coord A exon
chr11:113689918-113690230
Coord C2 exon
chr11:113689765-113689917
Length
313 bp
Sequences
Splice sites
5' ss Seq
CAGGTGTGG
5' ss Score
6.34
3' ss Seq
TCCATGCCTGGATCCCTTAGGGA
3' ss Score
6.97
Exon sequences
Seq C1 exon
CTTACAGCTCGGATATGCTCCAGGACACGGTGGTGCCCTTGTTCAGCACTCAGCTCTGCAACAGCTCTTGCGTGTACAGCGGAGCCCTCACCCCCCGCATGCTTTGCGCTGGCTACCTGGACGGAAGGGCTGATGCATGCCAG
Seq A exon
GTGTGGCCTGTGGTGGCTGGGGTGAGGGTGGGAGTGGAGGTGGGGGTGGGAGGGCAGGGGGCCTGCTGTGACTTGGCCCCCTGCCCTGGTCTGAGCTTGTCAGTGGTGTGAGACAGCCTCTCTAGAAGGAGGGGCACCTAGGCAAGTCTGGAGCTCATGCTAAGGGTTTAAGGAGGGGTGAGGCCAGCAGATATCTCAGCTAGAAGCAGGCGGGGCCCAGTAAGGAGATTCCACTTGCCATAGTGGTCTGGTGCTCTCCATCAGGAAGAACTAACTGGCTGTTTCTCTGTGTCTCCATGCCTGGATCCCTTAG
Seq C2 exon
GGAGATAGCGGGGGCCCCCTAGTGTGCCCAGATGGGGACACATGGCGCCTAGTGGGGGTGGTCAGCTGGGGGCGTGGCTGCGCAGAGCCCAATCACCCAGGTGTCTACGCCAAGGTAGCTGAGTTTCTGGACTGGATCCATGACACTGCTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000166682:ENST00000299882:11
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:
PF0008921=Trypsin=FE(20.3=100)
A:
NA
C2:
PF0008921=Trypsin=PD(19.5=88.2)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TACAGCTCGGATATGCTCCAGG
R:
CTGAGCAGTGTCATGGATCCA
Band lengths:
294-607
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains