Special

HsaINT0169735 @ hg19

Intron Retention

Gene
ENSG00000166682 | TMPRSS5
Description
transmembrane protease, serine 5 [Source:HGNC Symbol;Acc:14908]
Coordinates
chr11:113560953-113561661:-
Coord C1 exon
chr11:113561563-113561661
Coord A exon
chr11:113561096-113561562
Coord C2 exon
chr11:113560953-113561095
Length
467 bp
Sequences
Splice sites
5' ss Seq
ATAGTGAGT
5' ss Score
6.97
3' ss Seq
TTTCTCGGTGTCTCTCATAGCTT
3' ss Score
9.12
Exon sequences
Seq C1 exon
ACACTGTGGGCGCTGTGTGCCTGCCGGCCAAGGAACAGCATTTTCCGAAGGGCTCGCGGTGCTGGGTGTCTGGCTGGGGCCACACCCACCCTAGCCATA
Seq A exon
GTGAGTCAGCTCCCTGGGCCCTCGGTGCAGGGGCGGGTGTGGGAGGCATTCTTCCCCAGGGTGAGGCAAGGCCACATCCCCTGGCCACATGACAGTGCCAGCCCTGTTTTTCCCTGGCATCACCCTTGGTCAGGCCTAGGGTCTCCAGTCTCCCCTGCTTGGGCCTTTCTGGGGAGAACATCTACTGCAAGTTTTCCCTAAACCCAGACCCTTTTACTCCCCCTCCCCTTGTCCCAGGAGCGCCATGGTCTCACATTTGGTGTATGTGTGAGTCCTCCTGCTCTTCCCACTCCCAGCCCCCAAGTCCGATAGCCTACTGCTTCCTTGCTCAGCGTCCACAGCTCCCACCCTGGGCTCGCCTCTTTGGGTCTCCCTGTCTCTGGGACTTCGAATTACCTCCCCTCTTGCTGCTCTGCCTGCCTGGGCCTTGCTTTGTGCCCTGCAGTTTTTCTCGGTGTCTCTCATAG
Seq C2 exon
CTTACAGCTCGGATATGCTCCAGGACACGGTGGTGCCCTTGTTCAGCACTCAGCTCTGCAACAGCTCTTGCGTGTACAGCGGAGCCCTCACCCCCCGCATGCTTTGCGCTGGCTACCTGGACGGAAGGGCTGATGCATGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000166682-TMPRSS5:NM_030770:10
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:
PF0008921=Trypsin=FE(14.3=100)
A:
NA
C2:
PF0008921=Trypsin=FE(20.3=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CACTGTGGGCGCTGTGTG
R:
CTGGCATGCATCAGCCCTTC
Band lengths:
241-708
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