Special

RnoINT0039345 @ rn6

Intron Retention

Gene
Description
collagen type XX alpha 1 chain [Source:RGD Symbol;Acc:1563901]
Coordinates
chr3:176502260-176502869:+
Coord C1 exon
chr3:176502260-176502379
Coord A exon
chr3:176502380-176502704
Coord C2 exon
chr3:176502705-176502869
Length
325 bp
Sequences
Splice sites
5' ss Seq
CAGGTATGT
5' ss Score
9.8
3' ss Seq
TTGTCCCTCATATTTCCAAGGCC
3' ss Score
6.58
Exon sequences
Seq C1 exon
GTCTGACTCAGTACAGTGGAGACCCCCAGACCGAGTGGGACCTGAACTCCTTCCACACCAAGGAGCAAGTGCTAGCAGCAGTACACCACCTCCACTACAAAGGAGGAAACACGTTCACAG
Seq A exon
GTATGTCCTGGGCCTTGAGGTTTAGCTGTTCTAAAGCCTCTTGCCAACCCTTTTCTACCCTGTCCGTCCATGAACATTTGTGTGATGGGTGGGTGCTGAGCCCACTGCACACTTTACAGGTCAAAATCAACCACCACCACCCACCCCAACCTTTGGCAAACACGTGGAACTTTGGGCACCTTGTTGAGAGCAAGGGTCTGCATTGTTCAGAGGCGGCTTCTTTCTCGGTCCTACTTAGCAAGTGCCAGGATCAGCTGTGGTTGAGAGGGCGTCTGAGGTGGAGGTCCTAGTGGCCGTCCATCACTTTGTCCCTCATATTTCCAAG
Seq C2 exon
GCCTTGCCCTAACCCATGTGCTGGGGCAGAACCTGAAGCCAGCAGCAGGTGTCCGTCCAGAGGCAGCCAAAGTGTTGATTCTGGTGACAGACGGCAAGTCTCAGGATGATGTGCGCACAGCTGCCAGAGTCCTTAAGGACCAGGACATTGATGTCTTCACTGTGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000010326:ENSRNOT00000040270:7
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.098 A=NA C2=0.018
Domain overlap (PFAM):

C1:
PF0009223=VWA=FE(23.1=100)
A:
NA
C2:
PF0009223=VWA=FE(31.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
TGACTCAGTACAGTGGAGACCC
R:
ACATCAATGTCCTGGTCCTTAAGG
Band lengths:
271-596
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]