Special

HsaINT0169665 @ hg19

Intron Retention

Gene
ENSG00000137747 | TMPRSS13
Description
transmembrane protease, serine 13 [Source:HGNC Symbol;Acc:29808]
Coordinates
chr11:117774370-117774816:-
Coord C1 exon
chr11:117774674-117774816
Coord A exon
chr11:117774523-117774673
Coord C2 exon
chr11:117774370-117774522
Length
151 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
3' ss Seq
GTGCCCCCTCTCCCCTGCAGGGA
3' ss Score
11.77
Exon sequences
Seq C1 exon
ACAAGACATCCCCCTTCCTCCGGGAGGTGCAGGTCAATCTCATCGACTTCAAGAAATGCAATGACTACTTGGTCTATGACAGTTACCTTACCCCAAGGATGATGTGTGCTGGGGACCTTCGTGGGGGCAGAGACTCCTGCCAG
Seq A exon
GTGAGGGTACCTGTGGGTGGGGCTCAGGTCCCAGCACCCTGGGGATGGGGGAGGCAGGGGTGTTGGGGCTGATGTGGGAATTGGGACCCCACCCTTTCCCGCTCATGGACCACCTGTCCCATCCTGCGAATGTGCCCCCTCTCCCCTGCAG
Seq C2 exon
GGAGACAGCGGGGGGCCTCTTGTCTGTGAGCAGAACAACCGCTGGTACCTGGCAGGTGTCACCAGCTGGGGCACAGGCTGTGGCCAGAGAAACAAACCTGGTGTGTACACCAAAGTGACAGAAGTTCTTCCCTGGATTTACAGCAAGATGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137747-TMPRSS13:NM_001077263:11
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=0.035
Domain overlap (PFAM):

C1:
PF0008921=Trypsin=FE(20.5=100)
A:
NA
C2:
PF0008921=Trypsin=PD(19.7=88.2)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ACAAGACATCCCCCTTCCTCC
R:
ACCAGGTTTGTTTCTCTGGCC
Band lengths:
245-396
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains