HsaINT0169742 @ hg19
Intron Retention
Gene
ENSG00000166682 | TMPRSS5
Description
transmembrane protease, serine 5 [Source:HGNC Symbol;Acc:14908]
Coordinates
chr11:113566122-113567693:-
Coord C1 exon
chr11:113567580-113567693
Coord A exon
chr11:113566166-113567579
Coord C2 exon
chr11:113566122-113566165
Length
1414 bp
Sequences
Splice sites
5' ss Seq
CAGGTAGGA
5' ss Score
9.79
3' ss Seq
TTGGTACCTCTGTTTTGCAGGAA
3' ss Score
8.44
Exon sequences
Seq C1 exon
ACTCACTCACCACAAGGGAGTAAACCTCACTGACATCAAACTCAACAGTTCCCAGGAGTTTGCTCAGCTCTCTCCTAGACTGGGAGGCTTCCTGGAGGAGGCGTGGCAGCCCAG
Seq A exon
GTAGGACTACTGAGGCTGTTAGGTGAGTGGGGTCCCTTACTTCCTGGTGGTCAATCCAGCAAAAATCTCCTTTCTTGGGATGCCGGTGGGGAGGACACTGGTGGCCTATGATAGGAGGACAAAGAGGAACATTTCCTAGTTAGAAATTACAAACTCAGTTCACATGAGCCCTGTCTGTCACCACTTCACATCTGCTATTTGCCCTTCACAAGAAATGTAGGGTTGGTTATTATTGTCACAAGATTTGACATGGTACTCATCACCATTTTACAGGTTAGGAAACTGAGGCTTAATAAGGTTAAAGAGTCTTGTCCAAGGTCACATAAGTAATAAGCAGCTAAGTCAAGCCTTGAAACCAGGCTCCTGTCTCCAAGCTAAGTGCTCTCTGAATCCTGCCACACATTATTTGGATAATTCGGATATTTCAGGAAAGAGATGGTTGAGTTGCTCTGGCTAAGAGTTGCTTGTAGTCTGGAGAGTCTCCTAGAGAAGAGGGCTGTGGAATGGAGCAGCCCCTTCCCCAGATCCTGGGGATGGTTTGGTATGACTGGGGCACAAGCGGAGAGGGTCTTTGTGCCTTCCTAGGCTTCCTCAATCTGCCTATCAGCCTCCTGGGATAGAAAGGTGGGCACCCCCATTACCACATTTCCAATTTGAACTGTTCCTTCAGGCCCCTCCTGTCCAGCTCCTGTGCTCAGGAATGTGGCTGGAGTTGGGAAGGTTCTGACAGGGTTCTTGTCTTGGATACCTGAATGGGAAAATGGAAGTAGGGGTGGGGCTGACTCCTCCAGGAGAGCCGGGAGGGCTATGGATTTGGGAAACTAGGAGAAACTAAGAGGGTCTAGACATTGGACTGCTAGGGGCAAGAGGTGAGTAAAGAAAGAGAAGAGAGTTTTGGTCAAAAAAGGAACTAAGAGCTAAGAGAGAAGAGGGGAAAGAGGAGAGCAAGAATATGAATATGCAAAGCCCAGGCAGAGGGACCAGGGTGGAGAATACAGCAAACCTAGGAAGGAGCATGGGGTGAAGAACCCTAGTCACCCACACACTCACCTATCCGTTCATTCATTCATTGAGTGTGTATTCATTCAGGACACTTAGTGGGAACAGTGTGGCTTTCTCATCTGTAAACACACTATGTCCCAGTTGATCTGCAAGGACCATGAAGTCCTTCTGTTGCCCTCTGGGAGACTAGGCAGGAGGTGTGCTCCTGTCCTGGGGACCACTGATGAGGAGGGGTCTGAGTGTTTGGGTGGGGGCAGGAAGGAAATGGTGGTATTCTTCAGGCTGTGGCTACATGACAGCCTTAAGAACTGTCCACCACCCCCACCAGCCTCCCCCATTCTTCACGTCCTTGGATGTGTGTGGCTGCAGGGCGGCCCCTGCCCAGCTTCTTGTTGGTACCTCTGTTTTGCAG
Seq C2 exon
GAACAACTGCACTTCTGGTCAAGTTGTTTCCCTCAGATGCTCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000166682-TMPRSS5:NM_030770:6
Average complexity
IR-S
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=FE(38.8=100)
A:
NA
C2:
PF154941=SRCR_2=FE(15.3=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Genotype-Tissue Expression Project (GTEx)
- Autistic and control brains
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)