Special

RnoINT0015316 @ rn6

Intron Retention

Gene
Description
agrin [Source:RGD Symbol;Acc:2067]
Coordinates
chr5:173597115-173597741:-
Coord C1 exon
chr5:173597394-173597741
Coord A exon
chr5:173597308-173597393
Coord C2 exon
chr5:173597115-173597307
Length
86 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
3' ss Seq
ACTCTGTCTGTCTTCTGCAGTAC
3' ss Score
9.72
Exon sequences
Seq C1 exon
ACTGGTTTCCCACTTTCTTTACGGGAGCTGCAACAGGAACTACAGCTGCTATGGCCACAGCCAGAGCCACCACTGTGAGCCGACTGCCGGCCTCTTCCGTCACCCCACGAGTCTACCCCAGTCACACCAGCCGGCCTGTTGGCAGAACTACAGCACCACCAACCACTCGCCGGCCACCAACCACTGCCACCAACATGGACCGGCCTCGGACCCCAGGCCATCAACAGCCCTCAAAGTCCTGTGATTCCCAACCTTGCCTCCATGGAGGTACCTGCCAGGACCAGGATTCTGGCAAGGGTTTCACCTGCAGCTGTACTGCAGGCAGGGGTGGCTCTGTCTGTGAGAAAG
Seq A exon
GTGAGGTCACCCATTGCTAGAGGGTTTGGGGTTATGGCCAGAGGGTATAGCAGGGTCGTAGGTTTAACTCTGTCTGTCTTCTGCAG
Seq C2 exon
TACAACCCCCCTCCATGCCAGCTTTTAAGGGCCACTCCTTCTTGGCCTTCCCCACCCTCCGAGCCTACCACACACTGCGCCTAGCACTGGAATTCCGGGCTTTGGAGACAGAGGGACTGCTACTCTACAATGGCAATGCACGTGGCAAAGATTTCCTGGCTCTGGCTCTGTTGGATGGGCGTGTGCAGTTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000020205:ENSRNOT00000045678:23
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.641 A=NA C2=0.062
Domain overlap (PFAM):

C1:
PF0000822=EGF=WD(100=28.2)
A:
NA
C2:
PF0005418=Laminin_G_1=PU(25.0=50.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCCATCAACAGCCCTCAAAGT
R:
GGAGTGGCCCTTAAAAGCTGG
Band lengths:
170-256
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]