Special

GgaINT0132881 @ galGal3

Intron Retention

Gene
ENSGALG00000013781 | Q90WH5_CHICK
Description
NA
Coordinates
chr19:14921-15546:+
Coord C1 exon
chr19:14921-15310
Coord A exon
chr19:15311-15419
Coord C2 exon
chr19:15420-15546
Length
109 bp
Sequences
Splice sites
5' ss Seq
AAGGTAGGA
5' ss Score
9.45
3' ss Seq
CCTTCCCTTCCTTCTTCTAGACC
3' ss Score
11.26
Exon sequences
Seq C1 exon
GCACGGATTGAGGAGCTGGAGGAGGAACTAGAGGCAGAGCGGACGGGCCGGGCTAAGGTGGAGAAGCTGCGCTCAGAGCTGTTGCAGGAACTGGAGGAGACCAGTGAGCGGCTGGAGGAGGCAGGTGGTGCCACTTCAGTGCAGCTCGAGCTTAACAAGAAGCGGGAAGCCGAATTCCAGAAGCTGCGGAGGGACCTGGAGGAGGCCACATTGCAGCACGAGGCCACGGCTGCCACGCTGCGCAAGAAGCATGCTGACAGTGTAGCTGAGTTGAGTGAGCAGCTTGACAACCTGCAGCGTGTCAAGCAGAAGCTGGAGAAGGAGAAGAGTGAGCTCAAGCTGGAGCTGGATGATGTCAACTCCAACACGGAGCAGCTCATCAAGGCCAAG
Seq A exon
GTAGGAGACTGAGGCCTCAATGGCAAAAATCAAGATGAGGCTAGATGGGACAGTTATTCTTTCACACTTCCCATGTTCCCATGCATCTCCCTTCCCTTCCTTCTTCTAG
Seq C2 exon
ACCAACCTGGAGAAGATGTGCCGCACCACAGAAGACCAGATGAATGAGCACCGCAGCAAGTTGGAGGAGGCTCAGCGCACTGTCACTGACCTCAGCACCCAGCGAGCCAAGCTCCAGACAGAGAACA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000013781:ENSGALT00000040718:26
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.657 A=NA C2=1.000
Domain overlap (PFAM):

C1:
PF045827=Reo_sigmaC=PD(49.3=53.1),PF0157614=Myosin_tail_1=FE(37.7=100),PF079267=TPR_MLP1_2=PD(97.7=97.7),PF059116=DUF869=PU(29.4=36.9)
A:
NA
C2:
PF0157614=Myosin_tail_1=FE(12.3=100),PF059116=DUF869=FE(25.8=100),PF0205011=FliJ=PU(42.7=81.4),PF0003816=Filament=PU(34.5=88.4),PF0003816=Filament=PU(5.4=16.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Zebrafish
(danRer10)
LOW PSI
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GCTGAGTTGAGTGAGCAGCTT
R:
GTTCTCTGTCTGGAGCTTGGC
Band lengths:
252-361
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]