Special

GgaINT0000952 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chrE22C19W28_E50C23:9070-9794:-
Coord C1 exon
chrE22C19W28_E50C23:9564-9794
Coord A exon
chrE22C19W28_E50C23:9238-9563
Coord C2 exon
chrE22C19W28_E50C23:9070-9237
Length
326 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAAA
5' ss Score
8.38
3' ss Seq
ACACCGCTTTCCTTCTGCAGACA
3' ss Score
10.8
Exon sequences
Seq C1 exon
GTTTGCCACTTTTTGTGCAGCGGACCGTGGCTCGGACGATCGTCCTGCAGGAGATCATTGGGAAGGGCCGCTTTGGGGAGGTGTGGCGCGGCCGATGGCGCGGAGGTGACGTGGCTGTGAAGATCTTCTCTTCCCGTGAGGAACGTTCCTGGTTCAGGGAAGCAGAAATCTACCAAACCGTTATGCTGCGACATGAGAACATCCTGGGCTTCATTGCTGCAGACAACAAAG
Seq A exon
GTAAAACTGCTCAGCCCTGACAGCACAGACCCCATCGGCGTGCTGCTTCTGAGAGCTGCATCGCTTGGCTCACACGTGCAGTTAAGTGCTAAAGAAAGCCATCAGCATCCTGCTGCGTGTGCGAGTGTGTCCCACTGCAGGGTGGGAAGATGAAAACTGTTGCATAGAGACGTGTGTGTGTCGTGTGTACCTTAATGCTCCTCACCTGGCCTGCCCCAGGCTGGCTGCTGAGCTGCAGCCTTACCCAGTGGTTCTGTGTGCCAAAGGGATGCGCAGCGCTCAGCGGCTCTGCTCTGTCCCTGAGAAACACCGCTTTCCTTCTGCAG
Seq C2 exon
ACAACGGGACGTGGACACAGCTGTGGCTCGTCTCCGATTACCACGAGCACGGATCTCTCTTTGACTACCTGAACCGCTACACGGTGACCATAGAGGGGATGATCAAGCTTGCTCTGTCTGCTGCCAGCGGGCTGGCCCACCTGCACATGGAGATCGTGGGTACTCAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000014631:ENSGALT00000020492:4
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:
PF085157=TGF_beta_GS=PD(37.9=14.1),PF0006920=Pkinase=PU(22.2=82.1)
A:
NA
C2:
PF0006920=Pkinase=FE(19.4=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:
CGTCCTGCAGGAGATCATTGG
R:
GTACCCACGATCTCCATGTGC
Band lengths:
354-680
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]