Special

GgaINT0123774 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr17:8913482-8914077:-
Coord C1 exon
chr17:8913966-8914077
Coord A exon
chr17:8913547-8913965
Coord C2 exon
chr17:8913482-8913546
Length
419 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGA
5' ss Score
10.57
3' ss Seq
TGTCTCACACGTTTCCATGGAGA
3' ss Score
-0.2
Exon sequences
Seq C1 exon
GCTCTTTCCCAGCCTCAGCATCATCACAGAGCTGACCCATCCCTCCAACATGAGGTTCATGCAGTTCAGAGCAAAGGACAGCTACTCCTTAGCCCTTTCCAAGCTAGAGAAG
Seq A exon
GTAAGAGAAAGCTTTGCCTTCTGGGAATTCAGCACTGGGAGTCACTAATCCTGAGTTTGCTGTGGTCCTGTTCTCCTCCACACGCTTCACTCTGCATCCATCCAATATAACCTGCAGCAAACAAATACGTGGGTGGGTGATTTTGGGGCTGTCTGCCTCTTCCTACGTGTTTATGTGTTTCTTGGCTGCTGAAGGTTGTGCTGCTTTGCCTGCTGCTATGTTGGGAGCAGGGCAGTGAGTGAATGGGTGCAGGGATGCTCCAAGCAGGGAACCTCTGGGCTCAGCGCCGTGCCTGCAGCAGTGTCACTGTGCTGAGGTCTCCTGACAAGGGCAAACATCCCCAAGGCAGTGAGGCACGTGGAAACACCACATCCAGCCCGTAGCAAAATAAAGCCATGATGTCTCACACGTTTCCATGG
Seq C2 exon
AGAAAAAAAAAAAACTTCTTTCACCACAAAACCCTCTTTAAGGGCCTCCCTCCTGGCACGCCCAC
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000001645:ENSGALT00000038919:24
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:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]