Special

BtaINT0141583 @ bosTau6

Intron Retention

Gene
Description
suppression of tumorigenicity 14 (colon carcinoma) [Source:HGNC Symbol;Acc:HGNC:11344]
Coordinates
chr29:36961162-36961900:+
Coord C1 exon
chr29:36961162-36961242
Coord A exon
chr29:36961243-36961790
Coord C2 exon
chr29:36961791-36961900
Length
548 bp
Sequences
Splice sites
5' ss Seq
GAGGTGGGA
5' ss Score
4.3
3' ss Seq
AGCAGCATCTGTCTCCGCAGGTG
3' ss Score
8.52
Exon sequences
Seq C1 exon
CGGGCAGCCCAAGGGACATTTAACAGCCCCTACTATCCAGGCCACTACCCGCCCAACATCAACTGTACCTGGCACATCGAG
Seq A exon
GTGGGAGTTGTGAGCTGTGGGGGGTTAGAGAAGTTGGTTGGGGGGTAGATGGGGGAGGAGAGGAAGGGGTTGGGCGTGCTCCAGGGAGGCAGGAGAGAGGGCGATGAGCACCTTCGGCCACTCCCAAGGGGTGTGTGTGGAGGCTGTGGGCGGGGCAGTTTCCGAAGCAGCGTCTTCAGACCCAAGCCCAACCCCCCGTCCGTGGCCGGTGCCTGCTGGAGGGACCCAGCCCCGGGATGGGCTGGCTCTGGGGCCTCCTGGAGGAGCTGTGGGGACAGTGAGTGCCGTGCAGAGGAGGACACGCTCACTGGACGGCTGGAAACGCGCGCCATCCAGTCAGTGATGAGGGAGAACTGCCCGGCCTTCTTTAGAACACCACAGTGTGTGCTGCTGCTGGCGAGTCGGGAAGGTCTTCCTTCCAGATCCCTCCTGCCGTGTCCTCACTGCCCTGCAGGCGGGCGGGCGGGAAGAACGCCCCCATTCCCCACCAGCTCAGGAAAGAGGGAGGCTGTGCAGAGCCAGGCCCACAGCAGCATCTGTCTCCGCAG
Seq C2 exon
GTGCCCGACAACAAAAACGTGAAGGTGCGCTTCAAAGCCTTCTTCCTGCAGGAGCCCAATGTCCCCGTGGGCTCCTGCACCAAGGACTACGTGGAGATCAACGGGGAGAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000019712:ENSBTAT00000026272:16
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:
PF0043115=CUB=FE(25.0=100)
A:
NA
C2:
PF0043115=CUB=FE(34.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGGCAGCCCAAGGGACATTTA
R:
TTCTCCCCGTTGATCTCCACG
Band lengths:
190-738
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]