Special

GgaINT0000939 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chrE22C19W28_E50C23:454240-454653:+
Coord C1 exon
chrE22C19W28_E50C23:454240-454365
Coord A exon
chrE22C19W28_E50C23:454366-454471
Coord C2 exon
chrE22C19W28_E50C23:454472-454653
Length
106 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
3' ss Seq
CCCATCCTCTCCCACGCCAGGTG
3' ss Score
9.65
Exon sequences
Seq C1 exon
ACCCCCCCCCCTGAGCGGCTGGGCCCCCACGTTGGCTCCTCGGACACGTTGGATCTCATCAGCTCCAAGGACCTGGCCAGCCACCTCACCGACCACGACTGGAACCTCTTCAAGAGCATCCACCAG
Seq A exon
GTGAGGGCAGCACCTGGTTGCCAGGGGGGCTGGGGGGAGGGCAAACCCTCCGGGGTGATTCTGGGGGTCCCCCTGTCACGACCCCTCCCATCCTCTCCCACGCCAG
Seq C2 exon
GTGGAGATGATCCAGTACATCATGGGGCCACAGAAGTTCCACGAGGTGACGACGGCCAACCTGGAGCGAATGATGCGGCGTTTCAATGAGCTGCAGTACTGGGTGGCCACCGAGCTGTGCCTCTGCCCCGAGCTGGGCAGGAGAGCCCAACTGCTGCGCAAGTTCATCAAGCTGGCTGCACA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000006348:ENSGALT00000010260:15
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.190 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0061714=RasGEF=PU(12.9=57.1)
A:
NA
C2:
PF0061714=RasGEF=FE(32.3=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
TCATCAGCTCCAAGGACCTGG
R:
TGCAGCCAGCTTGATGAACTT
Band lengths:
251-357
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]