Special

RnoINT0046500 @ rn6

Intron Retention

Gene
Description
DENN domain containing 2D [Source:RGD Symbol;Acc:1305120]
Coordinates
chr2:209103211-209103970:+
Coord C1 exon
chr2:209103211-209103323
Coord A exon
chr2:209103324-209103900
Coord C2 exon
chr2:209103901-209103970
Length
577 bp
Sequences
Splice sites
5' ss Seq
CAGGTAACT
5' ss Score
8.63
3' ss Seq
TTGGTCTTCTCTCTCTTTAGGGA
3' ss Score
11.95
Exon sequences
Seq C1 exon
AGGGAGAACCTGCTCCGAGGTCAGCAGGAGGAGGAGGAACGGCTGCTCAAAGCCATCCCTTTGTTCTGCTTCCCTGATGGGAATGAGTGGGCACCGCTCACAGAGTATCCCAG
Seq A exon
GTAACTACTCAGCCTGCAGGCAAGGGTATCAGATTTGGAGGGAAGGGCAAATGTGTGGCTCCTGTCGTCCCCTCACCTGGTATGAATGCTGAGGTTTTGCCGGGGAAATATTTTGACTGGAATCCTTTGGCAAATGATTGAGGCTGTGACTTGACCTCTATCTGAAGACTTTTAAGAATCTCTTACCTGTTCCTAGAAGAAATAGACTCTTTTTTTTCACTCTGGACTGGAGAAAAAGACTTTGGCCTCTACAATATGGAAAAAGTCCTTACATCATGAACACTGGAAGTAGACCATGACTTCAAGTTTTAGATAAGAAGTAACCACAGAGCCTTACTTACCAGGTCTTTAAAGTGGTGATAATAATTTAACCTTCTTCAAAAAGGTTCAGTTGAGTCTCAAATGAGGCGATGAATTAGAGCTTGAATACCATCAAGTGCTTAGTGACTGTTGTGATTATCGCCATAATTAATCAGCGGCTCCCCCTTGTCTTCCTCTCCACTCCTCTAAAGCTGACGTCTATCTTGTTTTAGAATCTAGTGAGCAAATGCACACCATTGGTCTTCTCTCTCTTTAG
Seq C2 exon
GGAGACCTTCTCATTTGTCCTGACCAATGTGGATGGGAGCAGGAAGATCGGATACTGCAGGCGCCTCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000017680:ENSRNOT00000023807:3
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0345613=uDENN=FE(52.1=100)
A:
NA
C2:
PF0345613=uDENN=FE(32.4=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]