Special

GgaINT0092067 @ galGal4

Intron Retention

Gene
Description
desmoglein 2 [Source:HGNC Symbol;Acc:HGNC:3049]
Coordinates
chr2:105789783-105790275:+
Coord C1 exon
chr2:105789783-105789917
Coord A exon
chr2:105789918-105790089
Coord C2 exon
chr2:105790090-105790275
Length
172 bp
Sequences
Splice sites
5' ss Seq
GCAGTAAGT
5' ss Score
9.07
3' ss Seq
AAATCTTTTTATCCTTGCAGTTT
3' ss Score
8.18
Exon sequences
Seq C1 exon
ACACAAAGTAGCTATTCTTTGGTGGTGGAAGGGAAAGACCGTGGTGGTGCAGCAGATGGGAATGGTGCAACATGCTCTGTAGAAATCAAGATTTTGGATGTCAACGACAACCTGCCTGTGCTTGAAAGTTCTGCA
Seq A exon
GTAAGTACATTCACTTTACTTTTACTTTACAAGTACTTCACATGATATTTGGTGTGTTCATACACTTGCTGGTATCCCGTTGCTTAAGAAAACCTTATGCAGATTTTCTTGTACTGATGAAATGGGGTAGATCGGGACATCTTTTTACATTTAAATCTTTTTATCCTTGCAG
Seq C2 exon
TTTGAAGGAAGCGTTGAAGAAAACAGAGCAAATGTGGAAATTCTGAGAATAAAAGTATTTGATAAAGATGAGGAGTTTTCTGATAACTGGTTGGCAAACTTTTCATTTGTCTCTGGTAATGAAGGCGGTTATTTTCGTATAGTAACAGATACCAGAACAAATGAAGGAATTCTGACTCTTGTGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000015142:ENSGALT00000024433:6
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.067 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0002812=Cadherin=PD(32.0=68.9)
A:
NA
C2:
PF0002812=Cadherin=PU(58.7=98.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TTGGTGGTGGAAGGGAAAGAC
R:
CCGCCTTCATTACCAGAGACA
Band lengths:
245-417
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]