Special

RnoINT0139621 @ rn6

Intron Retention

Gene
Description
slit guidance ligand 1 [Source:RGD Symbol;Acc:69307]
Coordinates
chr1:260846673-260847418:-
Coord C1 exon
chr1:260847288-260847418
Coord A exon
chr1:260846828-260847287
Coord C2 exon
chr1:260846673-260846827
Length
460 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGA
5' ss Score
10.77
3' ss Seq
CCTCTCCTATTTCCTTCCAGTGC
3' ss Score
10.79
Exon sequences
Seq C1 exon
GTCTCCACAGCAGAGGACAATGGGATCCTCCTCTACAATGGGGATAATGACCACATTGCAGTTGAGCTGTACCAGGGCCATGTCCGTGTTAGCTACGACCCAGGCAGCTACCCCAGCTCTGCTATCTACAG
Seq A exon
GTAAGAATTTCTCAGGCTGTCAGCCTTCCTCGCTTGGGCATGCCGGGATGGGGCTTCTGGGTGGAGAGGTTGTGGGAACTACAGAAACATGGCTGACTAAGAAGAAAGGCCGCTTGGTTTCCTGAGTCTAGTCTACTAGTCTAGTCTAGGCTCCTCAACACTCATCTTTCCTGACCCAACCTCACCTCAGCCCCTCACTGGAGAAGAAGCTATCTCCAAATGTTTCAACCTTCCCTGGGCCTCAGGAAGGGGCAGTTGGGAGGCATCAGACCAAAGTCCACTTGGTCCCATTGGTTTTCTTCCTGAGGCCCACTCCCTGAGGCCCACTCTCTGAGGCCCACTCCCTGAGGCCCACTCCCTGAGGCTCACTCCCTGAGGTGGGCACCCACTCCCTGAGGTGGGTACCTACTCCCTGAGGCCCACTCCCTGAGGTAGGTACCCCTCTCCTATTTCCTTCCAG
Seq C2 exon
TGCTGAAACAATCAACGATGGGCAGTTCCACACAGTTGAGCTGGTGACCTTTGACCAGATGGTGAACCTCTCCATTGATGGTGGCAGCCCCATGACCATGGACAACTTTGGAAAGCACTACACACTCAACAGTGAGGCCCCCCTCTATGTGGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000026065:ENSRNOT00000034758:33
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.008 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0221019=Laminin_G_2=PU(33.3=97.7)
A:
NA
C2:
PF0221019=Laminin_G_2=FE(40.3=100)


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:
CTCCACAGCAGAGGACAATGG
R:
CACTGTTGAGTGTGTAGTGCT
Band lengths:
263-723
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]