Special

GgaINT0054956 @ galGal3

Intron Retention

Description
NA
Coordinates
chr5:15871311-15872244:-
Coord C1 exon
chr5:15872131-15872244
Coord A exon
chr5:15871491-15872130
Coord C2 exon
chr5:15871311-15871490
Length
640 bp
Sequences
Splice sites
5' ss Seq
GGGGTAAGT
5' ss Score
9.65
3' ss Seq
TTTTTCATTTCTTGTCCCAGAAC
3' ss Score
9.02
Exon sequences
Seq C1 exon
AACTACTGTGGCAGAAAAGGTCTGAATCAGGGAACCTTCAGAGTCATCACTGAGAACATTCCATGTGGCACAACAGGAACCACTTGCTCCAAGTCTATTAAAGTTTTCCTGGGG
Seq A exon
GTAAGTATGTTCTTCAGTAAGTTTCACCCCAAGCCTAATTTGCTGGAAGGACTGTTGGGTTGTCCTAGACAGACTGTATCATAAAAGCGTCCCCCAAGACAGTAGAAATGTTATCGCACTTCCATGCTCACTGCCAACAATTCTGCCAGGGAAAGCAATGGAGGGATTTTTGAATACAACATTTTGATGATAATATAAAATATCAAAAATGGTTACTAACAATATAGAAAACTGGACCTAACAGGTGACTTTTTAAATCAGTGTACAGTCAGCAAATGTACAATTAGAGTGGCATGGTTAAAATGGTAGTTTACAAGTTGTATAATTAGAAAGATTATTATGGTGGAAAGAGGTAATCAAAGATAAATGAAATGCTCACCTATGTCCTAGGCTCACAATAGAAAACTCCAAAGGGAGCAATCTCCAGAAAGAGATCCTTCCCTAGTGGCAGTCAGCCCTTAAATGAGGTCTAGGAGAGGTGCAGCCAGGCTTCACCCCTTCTGGTCACACAGCTGAATTGCCTTCTCCTGTGCTCCTGTGTCTGACTCAGTGCTTGCCTCAGGTGATCAATCAGTGGTTGAGGCCATGACTCAACAGTTCCCATACAATCAGTCTCTAACTTTTTCATTTCTTGTCCCAG
Seq C2 exon
AACTATGAGCTGGTACTCAGTGATGGACACTCTGATGTCATCCAGAGGTCACCTGGAGGAGAAATGCCATTTCAAATCCGTTCCATGGGCATCTACATGGTCGTTGACACTACTGTTGGTCTGATACTCATGTGGGACAAGAAAACCAGTATATTCATCAAACTTAGTCCCAGCTTTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000006740:ENSGALT00000010867:23
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:
PF0009420=VWD=FE(24.5=100)
A:
NA
C2:
PF0009420=VWD=FE(39.1=100)


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:
AACTACTGTGGCAGAAAAGGTCT
R:
CTGAAAGCTGGGACTAAGTTTGA
Band lengths:
294-934
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]