Special

HsaINT0046772 @ hg19

Intron Retention

Gene
ENSG00000162777 | DENND2D
Description
DENN/MADD domain containing 2D [Source:HGNC Symbol;Acc:26192]
Coordinates
chr1:111730753-111731408:-
Coord C1 exon
chr1:111731324-111731408
Coord A exon
chr1:111730993-111731323
Coord C2 exon
chr1:111730753-111730992
Length
331 bp
Sequences
Splice sites
5' ss Seq
AGAGTAAGT
5' ss Score
9.35
3' ss Seq
GGCCTTTATATCTCCTGCAGCTG
3' ss Score
8.86
Exon sequences
Seq C1 exon
GTTGGTGATGAAAAAGACATCCTGCCACCGAAGCTTCAGGATGACATCTTAGACTCTCTTGGTCAGGGGATCAATGAGTTAAAGA
Seq A exon
GTAAGTCCTTACTCTTATTTTGGGTCTCTCCAGGCAGTGCAAGGGCATGCTTCTCAATCATTCCCTTCCAGAACTAAAATGAACTCATTCAGTAGTCCTAGACCAGCCCTAGAGGCCTAGAACCTAGGGCAAGTCTGAATTTGGGATTGTATTCTTCCTAAGCAATGGCAGAGAACTCATACCCAGATTCCCATCTCAGTCAGTAATTATGAACCCTACCCTATGGCTTTCCCCAGGAGCTTTCCGCCTGCAAGAAAGCCATTCTTGAAGGTGAGTTTGGGTAATTTCATCCTTCTGCTACCCTCTGAGATGGCCTTTATATCTCCTGCAG
Seq C2 exon
CTGCAGAACAAATCAACGAGCATGTTTCAGGCCCCTTTGTGCAGTTCTTTGTCAAGATTGTGGGCCATTATGCTTCCTATATCAAGCGGGAGGCAAATGGGCAAGGCCACTTCCAAGAAAGATCCTTCTGTAAGGCTCTGACCTCCAAGACCAACCGCCGATTTGTGAAGAAGTTTGTGAAGACACAGCTCTTCTCACTTTTCATCCAGGAAGCCGAGAAGAGCAAGAATCCTCCTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162777-DENND2D:NM_024901:10
Average complexity
IR-S
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:
NO
A:
NA
C2:
PF0345514=dDENN=WD(100=84.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTTGGTGATGAAAAAGACATCCTGC
R:
AGGATTCTTGCTCTTCTCGGC
Band lengths:
318-649
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