Special

GgaINT0038642 @ galGal4

Intron Retention

Gene
Description
selectin E [Source:HGNC Symbol;Acc:HGNC:10718]
Coordinates
chr8:5100243-5100710:+
Coord C1 exon
chr8:5100243-5100425
Coord A exon
chr8:5100426-5100530
Coord C2 exon
chr8:5100531-5100710
Length
105 bp
Sequences
Splice sites
5' ss Seq
CAGGTATGT
5' ss Score
9.8
3' ss Seq
TGTTGTGATCTGTGTTGCAGCTG
3' ss Score
9.94
Exon sequences
Seq C1 exon
CTGTGACCTGCACTGTCTTAAAAGCACCTGCTAATGGCTCTCTGAACTGCTCCCGTTCCTCTGAGTTTACATGGAATACCACCTGTGAGTTCACTTGTGAGGAAGGATTTGCTCTGACAGGACAATCCACGCTGCACTGTGGCTCTTCTGGGGCCTGGGACAAGCAGCAGCCATCCTGTGCAG
Seq A exon
GTATGTTTTTCCATACCCACCTGAGCCCTTAGGGCTATCAGCATTGACTGGCATGTTGAGTTCCTGAGGCCTCTGTGCTGACTGCTGTTGTGATCTGTGTTGCAG
Seq C2 exon
CTGTGAGGTGTGATGCTGTAACCTGGCCAGAAGAAGGTTCTGTGAGCTGTTCTTATGCAGATCCCACCTATGGCTCACGTTGTGATTTCCGTTGCCGAGAAGGCTATGTCCTGGAGGGCCCATCCAGCACTGAGTGCATGGCACAGGGACAGTGGTCAGAGCCATTCCCAAAATGCAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000003399:ENSGALT00000005376:7
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:
PF0008415=Sushi=WD(100=91.9)
A:
NA
C2:
PF0008415=Sushi=WD(100=91.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCACCTGCTAATGGCTCTCTG
R:
GGCAACGGAAATCACAACGTG
Band lengths:
256-361
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]