Special

RnoINT0145622 @ rn6

Intron Retention

Gene
Description
syntaxin binding protein 1 [Source:RGD Symbol;Acc:3785]
Coordinates
chr3:11835770-11836452:-
Coord C1 exon
chr3:11836343-11836452
Coord A exon
chr3:11835872-11836342
Coord C2 exon
chr3:11835770-11835871
Length
471 bp
Sequences
Splice sites
5' ss Seq
GATGTAAGG
5' ss Score
6.35
3' ss Seq
TGGTGTGTGCTTGCATTCAGTCC
3' ss Score
6.25
Exon sequences
Seq C1 exon
GTATCACTGAAGAAAACCTAAACAAACTCATCCAGCACGCCCAGATCCCCCCAGAAGACAGTGAGATCATCACCAACATGGCTCACCTCGGGGTGCCCATCGTCACGGAT
Seq A exon
GTAAGGGCCAGGTCATAGGCAGGGAGACCGTGGGAGGTTGGCATACTGTATCCTCGCCACGTTCATGATTGACCAGACCAGTGACCGGCAGCTGGCGGCGTTTGGTGTTTTCAGTACCTGGGTCACAAAAGGCTCAAAACAGTAGAACTGGTTCATGTAAAACAGCCCGTGCTGCTGACATGAAAACATGAAACAGAAACCCAGGGCCACACACACACACACACACACACACACACACACACACACACTGTCTCAAACTCAAAAAACCCTGTCTCAAAGAATCAAAACAAAACAAAATCCCAGAAAACCCAGACTTTCTCAAGACTCCTTGTTTCAGAGTCTCTTGAGGAGGTCTATTTCAGAGCTACACCTCTCCTTTATTACTCTTTGCCAATGCTAAGCGGGTCCTTAAGAGAATTCCTAGAAGTCGCTGAGACCCATCTAACTGACCTGGTGTGTGCTTGCATTCAG
Seq C2 exon
TCCACACTACGCCGCAGAAGCAAGCCGGAGCGGAAGGAGCGCATCAGTGAGCAGACCTACCAGCTCTCACGATGGACCCCGATCATTAAAGACATTATGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000015420:ENSRNOT00000021178:15
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.135 A=NA C2=0.382
Domain overlap (PFAM):

C1:
PF0099518=Sec1=FE(6.5=100)
A:
NA
C2:
PF0099518=Sec1=FE(5.9=100)


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:
CACTGAAGAAAACCTAAACAAACTCA
R:
TCCATAATGTCTTTAATGATCGGGGT
Band lengths:
207-678
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]