Special

RnoEX6035526 @ rn6

Exon Skipping

Gene
ENSRNOG00000016397 | Tmprss13
Description
transmembrane serine protease 13 [Source:RGD Symbol;Acc:1310872]
Coordinates
chr8:49646328-49648708:+
Coord C1 exon
chr8:49646328-49646426
Coord A exon
chr8:49648258-49648400
Coord C2 exon
chr8:49648556-49648708
Length
143 bp
Sequences
Splice sites
3' ss Seq
CCACATTCTCCTCACTGAAGAGA
3' ss Score
2.64
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
Exon sequences
Seq C1 exon
CTCACATCCACCCTGCCTGCCTCCCTTTGCATGGGCAGACCTTCGGCCTCAATGAGACCTGTTGGATCACTGGCTTTGGCAAAACCAAGGAAACAGATG
Seq A exon
AGAAGACATCTCCCTTCCTCCGAGAGGTTCAGGTCAACCTCATCGACTTCAAGAAGTGCAATGACTACTTGGTCTATGACAGTTACCTTACCCCAAGGATGATGTGTGCGGGGGACCTTCGAGGAGGCAGGGACTCCTGCCAG
Seq C2 exon
GGAGACAGTGGAGGACCCCTCGTCTGTGAGCAGAACAACCGCTGGTACCTGGCAGGAGTCACCAGCTGGGGCACAGGCTGTGGCCAGAAAAACAAGCCTGGGGTGTACACCAAAGTGACAGAAGTACTTCCCTGGATCTATAGAAAGATGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000016397-'13-14,'13-13,14-14=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

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

C1:
PF0008921=Trypsin=FE(14.4=100)
A:
PF0008921=Trypsin=FE(20.5=100)
C2:
PF0008921=Trypsin=PD(19.7=88.2)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTCACATCCACCCTGCCTG
R:
TCCATCTTTCTATAGATCCAGGGA
Band lengths:
251-394
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]