Special

HsaINT0052436 @ hg19

Intron Retention

Gene
Description
desmoglein 2 [Source:HGNC Symbol;Acc:3049]
Coordinates
chr18:29104411-29104851:+
Coord C1 exon
chr18:29104411-29104548
Coord A exon
chr18:29104549-29104665
Coord C2 exon
chr18:29104666-29104851
Length
117 bp
Sequences
Splice sites
5' ss Seq
GTGGTAACT
5' ss Score
5.08
3' ss Seq
CATGTGTTCATGTTTTGCAGCTT
3' ss Score
9.28
Exon sequences
Seq C1 exon
GAACACAGCAGCTACACTTTGACAGTAGAAGCAAGAGATGGCAATGGAGAAGTTACAGACAAACCTGTAAAACAAGCTCAAGTTCAGATTCGTATTTTGGATGTCAATGACAATATACCTGTAGTAGAAAATAAAGTG
Seq A exon
GTAACTATTATTCTTCTAATAACTGTACCTATTTATTTATATTTCAGTCCTAATTAAAAATATATCACTTATATTTGTATTTCATTGAAATAAAAATCATGTGTTCATGTTTTGCAG
Seq C2 exon
CTTGAAGGGATGGTTGAAGAAAATCAAGTCAACGTAGAAGTTACGCGCATAAAAGTGTTCGATGCAGATGAAATAGGTTCTGATAATTGGCTGGCAAATTTTACATTTGCATCAGGAAATGAAGGAGGTTATTTCCACATAGAAACAGATGCTCAAACTAACGAAGGAATTGTGACCCTTATTAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000046604-DSG2:NM_001943:7
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.370 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0002812=Cadherin=PD(32.0=69.6)
A:
NA
C2:
PF0002812=Cadherin=PU(59.4=96.8)


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:
AGAAGCAAGAGATGGCAATGGA
R:
AACCTCCTTCATTTCCTGATGCA
Band lengths:
242-359
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development