Special

GgaINT0133400 @ galGal4

Intron Retention

Gene
Description
agrin [Source:RefSeq peptide;Acc:NP_990858]
Coordinates
chr21:2716785-2717289:-
Coord C1 exon
chr21:2717273-2717289
Coord A exon
chr21:2716950-2717272
Coord C2 exon
chr21:2716785-2716949
Length
323 bp
Sequences
Splice sites
5' ss Seq
TAAGTGCTC
5' ss Score
-8.84
3' ss Seq
TGTCATCCTTCTCTCCTCAGGGA
3' ss Score
12.61
Exon sequences
Seq C1 exon
TTCCTGACCTGCAGTAA
Seq A exon
GTGCTCAGGAGTGTGTTGCCAATAGCAAAACCTTGGAGATTTTATCTAGAGGGACTGGAATTACTGGAATTGCTGTTGCCAGCAATGATGTGCCAAGGTGCCTGGTGCTGCAGTGGGCTGGGTGAGCACTGCAGGCTGGCATCCTGAAGGTGGCATATGTCTCTCCTGCATGGCAGTTCTGCCTGTAGGGTCAATGGGTGGCATCCCTAAGAGATCTGTGGGACCAGGCAGGCAGATGTCTCCAGGGCCCTTTGCACAGGGGTGGACGAAGAGAGTCTGTGGGCAGCTGGTTTGGAGGGTATCTGTCATCCTTCTCTCCTCAG
Seq C2 exon
GGACAAAATGTCCATGGAAGTGGTGTTCCTGGCCAAGAGTCCCAGTGGCATGATCTTCTACAATGGGCAGAAGACAGATGGCAAAGGAGACTTTGTGTCTCTGGCTTTGCACGACGGCTACCTGGAGTATCGATATGACCTGGGCAAAGGGGCAGCTGTGCTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000002041:ENSGALT00000003171:31
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:
NO
A:
NA
C2:
PF0005418=Laminin_G_1=PU(33.8=82.1)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]