Special

HsaINT0046713 @ hg38

Intron Retention

Gene
ENSG00000213047 | DENND1B
Description
DENN domain containing 1B [Source:HGNC Symbol;Acc:HGNC:28404]
Coordinates
chr1:197645690-197647114:-
Coord C1 exon
chr1:197647055-197647114
Coord A exon
chr1:197645744-197647054
Coord C2 exon
chr1:197645690-197645743
Length
1311 bp
Sequences
Splice sites
5' ss Seq
CCGGTGAGT
5' ss Score
10.9
3' ss Seq
GATTTATTTGTATTGATTAGCAT
3' ss Score
3.31
Exon sequences
Seq C1 exon
AACCAAGAGATATTTATTGCCTGTGAGCAAGTTCTGAAAGATCAGCCTGCTCTAGTACCG
Seq A exon
GTGAGTTAAAAGGACATTGGCTTCTAAAAATCACTATTAAATAGGAAAAATAATCACTTATTTCACTATGCCTTTAAGCTTCACTCCAGCCCTTTGGGAAATGGTGAATTTGACTCTTAAGAAAATTAATCATTTGGAATATATAATATTTTCTGTTTATACTATCTTTTAAAGCATAGTTTTATGAAATATAGTACTATTAAAAACTATTCCAAATAAAAGTAGGTTATAGAGACCGAAATCTTTGCATATTCTCCATTTTCAGTAGTAGTAATTTTAAAGTATATTCACAGCACAAGATTTGTCACATTTTTTGGTCCCAAGATCACAAAAGATCTTGTGATTTATCTCCTATTGTTCTTCTACCCTGGAAAATTATAGATTATGACTGTGTTAACTATCCTTGTTCTGACTAGTTCAACTGTGCTCAAATATTGGCTAAAATGTTTCTTTTCTAATCATTAATAATAAGATATTATTAAATATGTCCTTATGTGATTCAGATATTAAATAATTTTGGAGATTAATATGAACAGAAAATAAAACTTTTGATGATTAAATTGCACTTTGATTCTGGGTGGTAAAATTTGGGAACATTGTGGGAAACATGAAGGCATATATACACAATGTATTCTTTATGTAAGTATTCTGATGAACTGTTTTACTTCTTTGAACATTATAGAAGCTAATTAATATTTGGCAGATGTGTAACAATCATATTTTGGGATTACTACGTGTTTAAGAAATTTTAAACATTGAAAAATTATGCTTTATTGCTATTTGCTAAATAATAGGGTGGTTGATGTTTACAAAAGAGATTTCTTGTGACTTACCATAGAAACCCAGCCCAGGAATCTTAGTAGATTTTGATATATTTGGTTAGCAAGCTTTAATTTTTCCAGTCCACCTCAACTAAATGTGTTTTAATAATATATATGTTTATATGTATGTATAGGTGTGTATGTCTCTATATACTGTATATATACACATACGTGTATATGTATATATGTACAAAATAAACCTTTCAGCAATATACTCTTTTTTTGCCTTAACATTTTTTCCCTATTTTAATTTTAATTTTAGGGTCAAATATTTTTAACCAAGTCTTAACTTTTTGTATGGCAATGTAATTGTTAAATCTCATATAAACCCGCTAACTCATTTAAGAATCTCTCAAATTCAACAAATCCTGAATGTCAGTCCATGGCATTTTTTAATTTACTCAATATATTTTTTTCTGATTTTCATTACAAATTATATGTTACCAGTTTTAATTATCTTTTTCATATGTGATTTATTTGTATTGATTAG
Seq C2 exon
CATTCCTACTTCATTGCCCCTGATGTAACTGGACTCCCAACAATACCCGAGAGT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000213047:ENST00000620048:8
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:
PF0214116=DENN=FE(9.5=100)
A:
NA
C2:
PF0214116=DENN=FE(18.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Chicken
(galGal4)
ALTERNATIVE
Chicken
(galGal3)
No conservation detected
Zebrafish
(danRer10)
LOW PSI
Fruitfly
(dm6)
No conservation detected
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]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development