Special

RnoINT0040495 @ rn6

Intron Retention

Gene
Description
collagen type IX alpha 3 chain [Source:RGD Symbol;Acc:1310255]
Coordinates
chr3:176111025-176111812:+
Coord C1 exon
chr3:176111025-176111078
Coord A exon
chr3:176111079-176111758
Coord C2 exon
chr3:176111759-176111812
Length
680 bp
Sequences
Splice sites
5' ss Seq
CTGGTAAGT
5' ss Score
10.65
3' ss Seq
CTGTCCCATGTTTCCTTTAGGGC
3' ss Score
10.72
Exon sequences
Seq C1 exon
GGTGACAGGGGTGATAGGGGACCAGAAGGGTTCCGTGGCCCTAAGGGTGACCTG
Seq A exon
GTAAGTGAGAGGGAGCTTGGTTCTCTGGACTTTTCTATGAAGAGGCTGATCTAACTTCTGTAGCTGGGGGTGGAGGATACTTAGAGGTCCCTGCTAGGGGCATGAAGGCCCTCTCCCTGTCCCCCCAAAACACCCAAAGCTTATCTGGAAGACTTTGGGCCTCTCCTGAGCAGCCAGCAGTGAAGAGCTCTGAGCAGAGGCTGGGGAATGGGCCACTGAGCTCAAATCCTAACTCTAGTCCAGCCCTGGGTGCTAGGCAGACGTTTCTTTTCTGCACCTCACTGTCTCAAACTGCCCTGCTACAGACGGAGGCTCTGCAGTGAGGCACGGGGACAGGAGCTAAGTAGACACTCACCCAGGTTTCTCCTGAACAGAAGTGGCTATCGCCAAACATGCAGCCTCCAAACCTCTTCTTCCCCACCCAAGACCAGTGGCTGAGCAGTGCCACAGTGACCACAACTCATAAGATTGCCCCATGAGTAGGGTCCTCAACAGGCCCTGGTGATGGAACCTAGCTCTGGGTTGGGATGAGCCATGACGCTTTCCCCAGGGGAAGCACAGTATACCTGATGTACCAAAAGCTGGGCCCATGTGGCTGAGCCTGTGGGGACATGGTGAGGCAGGATGGGATGTCCCTTGGGGTCTCAACTATAGCTGCTTCTGTCCCATGTTTCCTTTAG
Seq C2 exon
GGCAGGCCTGGTCCCAAAGGAATCCCTGGAGTGGCTGGGCCAGGCGGAGAACCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000009531:ENSRNOT00000013105:16
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=NA C2=1.000
Domain overlap (PFAM):

C1:
PF0139113=Collagen=FE(21.5=100),PF0139113=Collagen=PU(18.5=94.4)
A:
NA
C2:
PF0139113=Collagen=FE(21.5=100),PF0139113=Collagen=FE(18.5=100)


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:
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]