Special

GgaINT0000899 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chrE22C19W28_E50C23:54301-54778:-
Coord C1 exon
chrE22C19W28_E50C23:54725-54778
Coord A exon
chrE22C19W28_E50C23:54439-54724
Coord C2 exon
chrE22C19W28_E50C23:54301-54438
Length
286 bp
Sequences
Splice sites
5' ss Seq
AAGGTACAG
5' ss Score
8.04
3' ss Seq
TCTTCTCATTTCCCATTCAGCAA
3' ss Score
8.04
Exon sequences
Seq C1 exon
GCAACATTCAAGGGCTGGATGGACATCATGTATGCAGCAGTAGATTCCAGAAAG
Seq A exon
GTACAGTGCATGGCCACAAGCACTCTTACCCCCCAGCAAAAATGGTAGAGCTGTGTTTATATCATGTATTTCATTTCGTTATAGCGTGGTTTTTCATTTGCTGGTGTTGCTGTGGTAAGTTAAAAGATGCTGGAGCAAATCCCCGAAAGAGCATTTGTTTGGTTGCTTTATTAAGGGCAGGGAAACTCCTGATTGCCTAAAAATACACTGAAAAAGATCTCATTTTGACTCCATGGGTAAGATGTCTTTGCAATGTCATTTCCTTCTCTTCTCATTTCCCATTCAG
Seq C2 exon
CAAGAAGAGCAACCCAAGTACGAGGACAACATCTACATGTACATATATTTTGTTATCTTCATCATCTTTGGCTCCTTTTTCACTCTGAACTTGTTCATCGGTGTCATCATTGACAACTTCAATCAACAAAAGAAAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000006060:ENSGALT00000009776:23
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:
PF0052026=Ion_trans=FE(7.4=100)
A:
NA
C2:
PF0052026=Ion_trans=PD(15.2=76.1)


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:
GCAACATTCAAGGGCTGGATG
R:
TTTTCTTTTGTTGATTGAAGTTGTCA
Band lengths:
190-476
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]