Special

RnoINT0051397 @ rn6

Intron Retention

Gene
Description
desmoglein 2 [Source:RGD Symbol;Acc:1311143]
Coordinates
chr18:15598546-15599199:-
Coord C1 exon
chr18:15599057-15599199
Coord A exon
chr18:15598774-15599056
Coord C2 exon
chr18:15598546-15598773
Length
283 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGT
5' ss Score
11
3' ss Seq
CTCTCCTGCTTGCTTTCAAGGTC
3' ss Score
10.43
Exon sequences
Seq C1 exon
GTACGTAAAAGTGCAAGACACCGACAACTGGGTCTCTGTGGACTCTGAAACTTCAGAGATTAAGCTGGTAAAGATTCCCGACTTTGAATCTCGACACGTCCAGAATGGCACCTACACTGTAAAGGTTGTCGCTATATCCAAAG
Seq A exon
GTAAGTCAAATAAGCACATGGTTTTCGTGGTTAAATGCATTTAGATTTTAACTTCCGCCACCAGAAGTGTTTGTTCTGACTGTGTATAAAGGGCTCATCTCGTCAGTGCGCCTGCCCATTTTTGCTTATTTTGTGACTTCGCACTGATAGGAACCTGAGAGCCAGCTGTGGGGGTTATCCCAATGCCTAGCACCCACTCTTTATCTGATTGGCTTCTGGACTGACCTGTGTCTATGGTCGGTGATGCACTCAGAGTCTGAACTCTCTCCTGCTTGCTTTCAAG
Seq C2 exon
GTCACCCTCAAAAAACCGTCACTGGCACCATCCTTATCAATGTTGAAGACGTCAATGACAACTGTCCCGTACTGGTGGACTCAGTACGGAGTGTCTGTGCGGATGCACCGTATGTGAACGTCACTGCGGAAGACTTGGATGGACCCCGGAACAGTGGGCCATTCACCTTCTCCATCATTGACCAGCCTCCCGGAACGGCACAGAAGTGGAAAATCACGCACCAAGAAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000016526:ENSRNOT00000022270:10
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=0.013
Domain overlap (PFAM):

C1:
PF0002812=Cadherin=FE(51.1=100)
A:
NA
C2:
PF0002812=Cadherin=PD(16.0=19.5)


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:
CAAGACACCGACAACTGGGTC
R:
GAGAAGGTGAATGGCCCACTG
Band lengths:
302-585
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]