Special

GgaINT0069613 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr4:64990448-64991383:-
Coord C1 exon
chr4:64991309-64991383
Coord A exon
chr4:64990563-64991308
Coord C2 exon
chr4:64990448-64990562
Length
746 bp
Sequences
Splice sites
5' ss Seq
CATGTAAGT
5' ss Score
8.31
3' ss Seq
AGTTATTCTTGTATTTACAGCTT
3' ss Score
6.66
Exon sequences
Seq C1 exon
CATTGCAGAAATTCAGAAAGATGTGGAATATCGACTGCCGTTCACTGTAAACAACTTCACAATTAATATTAACAT
Seq A exon
GTAAGTAGAATGGGATCTCTCTAAATGCACGTCTGAAAAATTATATATATTTTTTATGTTCCATTATGGTAATGGAACATAAGGAAGTCCATCTCATAACTAATTTCAGGAACTACTGCCCCAATTTGCCTTAGTAGTCTTAGTAATCTGAGTGAAACTTGCTCTGTCCATGATGCACATGCTCAGGTCAAAGCCTAATTATATTTTGCCATGCTCAGTTCCTTACCACAGTGAAGCTTCTGGATCAGAGTTTGAAAGTGATTTGTTGTAATATACCCTATGAATTTGCTTGTGGTGAGGGGGTGCTTCTGCTTTGGTAAATGTTGATAACATTCAATTCTCAGGTTTTTTATTACTCAGCCCCCCAGTTTTGCTAACTTACCTGATACTCTTGCAAGCTACGCTGCATTGCCTTTAGAGTAATACAATTTGTGTGAAAGTATTCTCAACACATTATAGCTTCTCCTCTGTCAGTGGACATAATTGCATCACTGTTATCCTACAGCTCTTCTCAGTAAATGCTCTTGTGTTCCATGAAAATGTAGTATTCTAATCTCTGTGAAGTTTCATTACTGACTTCTGATTTTGTAGCTGAATAATCTTCTCTTGTACTCCATGCTGTATCTCTGTACCTTTTTTTCATAGAAGAGTGTGGTTATGTGAATTACTGTGTTTTTTCCTTGCATAAGAAGCCTTCTAAAAGCACACTTTACGGGGTATAGTAACAGTTATTCTTGTATTTACAG
Seq C2 exon
CTTGCTTCCGCCTCAGTTTCCTCAGGAAAAACCAGTCATCAGTGTTTTCCCACCTGTGAGACATCACCTGATGGACAAGCAGGGAGTATATGTGACTGGTCCATTAATAAACAAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000013646:ENSGALT00000022194:2
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:
PF057438=UEV=PU(22.2=69.2)
A:
NA
C2:
PF057438=UEV=FE(46.9=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CATTGCAGAAATTCAGAAAGATGTGG
R:
ATTGTTTATTAATGGACCAGTCACAT
Band lengths:
190-936
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]