Special

RnoINT0103716 @ rn6

Intron Retention

Gene
Description
netrin 5 [Source:RGD Symbol;Acc:1565197]
Coordinates
chr1:101674560-101675083:+
Coord C1 exon
chr1:101674560-101674709
Coord A exon
chr1:101674710-101675029
Coord C2 exon
chr1:101675030-101675083
Length
320 bp
Sequences
Splice sites
5' ss Seq
AACGTGAGT
5' ss Score
9.54
3' ss Seq
TTTCTCCTCTCCTCTGACAGGAA
3' ss Score
11.7
Exon sequences
Seq C1 exon
CCTGCCAGTGTCACCCAATTGGAGCAACAGGAGGGATGTGCAACCAGACCAGTGGCCAGTGCTCCTGCAAGTTAGGGGTCACGGGCCTGACATGCAATCACTGTGGTCCTGGGTACCAGCAGAGCCGCTCACCCAGGATGCCCTGTCAAC
Seq A exon
GTGAGTCCTATAGCACGTAAAGCCGTCAGTCCTGAACTGGGGTGGGGGAATGACAGTCCAGGTCTCAGGGGACAACTGCAGTGTGTGGCTTTGGTTTGGGGGTGGCAATGGATGAACCCTGAATCCTCCAAGAATTCGGGCTGGGAACTACAGACTCTTCAGTCTTGGGAAGAAGGCTGAGGTTCTGGACTCCTGTTCTTATGAGGGGAGGGGAGGGTCCTGGTGAGGATGAAGGATGGTTGTACCCTTGAGAGTTGTTTGCCTGGATTCCTAGTGGTGATTCCTAGAGTTTAAGATGTGTTTCTCCTCTCCTCTGACAG
Seq C2 exon
GAATTCCAGAAGCAACAACTGCCCTTGCTACTACTCCTGTTGCATCGCGATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000021016:ENSRNOT00000028524:3
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.039 A=NA C2=0.158
Domain overlap (PFAM):

C1:
PF0005319=Laminin_EGF=WD(100=96.1)
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CAGTGTCACCCAATTGGAGCA
R:
CTGATCGCGATGCAACAGGAG
Band lengths:
199-519
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]