Special

GgaINT0011789 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr20:7827789-7828462:-
Coord C1 exon
chr20:7828322-7828462
Coord A exon
chr20:7827951-7828321
Coord C2 exon
chr20:7827789-7827950
Length
371 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGG
5' ss Score
8.41
3' ss Seq
TGCTTGATCTTCCCCCGCAGTTC
3' ss Score
10.16
Exon sequences
Seq C1 exon
GAAAATGTGGAGGGTCCGAGGTGTGACCAGTGCCGCCTGGGGACGTTTTCTTTGGATGCCAGCAACCCCAAGGGGTGCACCAAGTGTTTCTGCTTTGGTGCCACCAATCGCTGCCGCAGTGCTGTGAAGTACCGAGCTGAG
Seq A exon
GTGAGGGATCAGCAGAGCGGCTGTGCTCTTTTCTTGGGTCTTCATTGTGCACTAGTCTTACCCTGCTGGAAGATACAGTGTGAAGAGTGTTATCTTTGTCCTACTATGCCCCTCTCCCATTTTCAGCCCTTTTCCTGGTCTCTGGAGTCTCAGAGGGTAGAAAGTCATGGATGGCATTTGGGGATTATGCCAGGCAAGGGTGGTGCTCAGTTTTCCAGTGGCTTCATCAGGATGTGTGTGAGGCTGTGACCCTGTTGGCATCTTTTCAGCCGCGCTGAGAATTGCTCTTCTAAGCATCAGCATCCAAATGCCTTCTGTAGCTCCTCCAGGGCACAAAGGGAGAAACACGTATGCTTGATCTTCCCCCGCAG
Seq C2 exon
TTCATCGACATGAATGGCTGGCTCTTGATGAGCAGTGACCGCCAGGAGGTGCCAACAGCCCTGAGCCTGCGGGAGCAGCTGCTCCGTGCTGATCTCAGGAACCTCCTGGATGCCTATCAGGAGCTCTACTGGGTTGCACCTAGCTCCTACCTTGGGGACCGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005321:ENSGALT00000008535:38
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:
PF0005319=Laminin_EGF=PD(51.0=53.2)
A:
NA
C2:
PF0005213=Laminin_B=PU(8.0=20.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GAAAATGTGGAGGGTCCGAGG
R:
CGGTCCCCAAGGTAGGAGCTA
Band lengths:
302-673
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]