Special

GgaINT0134973 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr21:992944-993463:+
Coord C1 exon
chr21:992944-993075
Coord A exon
chr21:993076-993334
Coord C2 exon
chr21:993335-993463
Length
259 bp
Sequences
Splice sites
5' ss Seq
AGCGTGAGT
5' ss Score
8.2
3' ss Seq
GCTCTTTGCTCTCTCCCCAGGTT
3' ss Score
11.28
Exon sequences
Seq C1 exon
GCTGTGCTGTGGGGCGTTGGGGTCCGGGCTGTGCCAACGTCTGCGAGTGCAGCAGCAGCACCGGGAGCTGCGATGCGGTGACGGGGCAGTGCGCCTGCGATGCCGGCTACACGGGCAGCCGCTGCGAGGAGC
Seq A exon
GTGAGTGTGTGCTGCAGTGTGTTTGGGCTCAGCTTTGTCTCCCACAGCTCTGTGGGAAGCGTTGGTGCCATGGCAGAGGGAATTGCATCCCTGCGATGCTGTCCTGGGGTGGGTGTGTGGGTACATCTGTGAGCGGCGGACCCTCATTTTAAACACGAGGCAGCCATATCCTTACAGATCCCTTTTGTCCCAGCCTGAGCTCCCATTGCAGCACAGCCTCCCAAGGACAGCTTCCCAGTGCTCTTTGCTCTCTCCCCAG
Seq C2 exon
GTTGCCCGGCAGGATGGTTCGGGTTGGGCTGCCGGCGCCGCTGCCAGTGTGAGCACGGGGCTATGTGTGACCACGTCAGTGGGGCATGCACATGTGCTGAGGGCTGGAGGGGGACCTTCTGTGAGCACC
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000001040:ENSGALT00000001544:19
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:
PF0005319=Laminin_EGF=PU(63.8=66.7)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(34.0=36.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CTGTGCTGTGGGGCGTTG
R:
GGTGCTCACAGAAGGTCCCC
Band lengths:
260-519
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]