Special

GgaINT0000884 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chrE22C19W28_E50C23:73864-74496:-
Coord C1 exon
chrE22C19W28_E50C23:74433-74496
Coord A exon
chrE22C19W28_E50C23:74006-74432
Coord C2 exon
chrE22C19W28_E50C23:73864-74005
Length
427 bp
Sequences
Splice sites
5' ss Seq
AGGGTGAGT
5' ss Score
9.25
3' ss Seq
CTCTTCCCTCCTCTCCGCAGTCA
3' ss Score
11.52
Exon sequences
Seq C1 exon
CAAATTTTTACATAATTCCTGGTGCCCCTGATCCTTTGCTCTGTGGTAACAGCTCCGATGCAGG
Seq A exon
GTGAGTGGTTGAGCTTTATTAAGAGGAATGACTAATTACCACTGATGTTCGCTAATGATGACAAAACCTTTGGAATGTTTCCTGTTGCTTTGCTTTGTTGGTTCTGGTGTTATTTCAAACGTGAAATGTAAATGTTTCACATTCGTTAATCTAATTGTGAAGCCATTGTTGCTGTCTGTCGCACTGATGCGATGTGAGCTGGCATTTCTGGTTTCACCTCCAGGGGATGGAACACCCAATGATGATGACTGGTGGCAATAATTCCTTCTGAGTCCCATCAGAGAAATCAGGGATGGAGGCTCAGAAACAGAAACTTTCCATGTGCCATTGCCTCCAGTTGGTCGTCACAGTCAATGTGCATGTGATGGATTTGCCCTGTCCCTTTTGCTGCATCAGTGCCCTGAAATCTCTTCCCTCCTCTCCGCAG
Seq C2 exon
TCAATGTCCAGAGGGTTACACATGCATGAAAGCAGGACGGAACCCAAACTACGGTTACACGAGCTTTGACACTTTCAGCTGGGCTTTCCTGGCTCTGTTTCGCCTTATGACTCAGGACTTTTGGGAAAACTTGTATCAATTA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000006060:ENSGALT00000009776:8
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(8.4=100)
A:
NA
C2:
PF0052026=Ion_trans=FE(18.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
TTTTTACATAATTCCTGGTGCCCCT
R:
TGATACAAGTTTTCCCAAAAGTCCTG
Band lengths:
198-625
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]