HsaINT0046779 @ hg38
Intron Retention
Gene
ENSG00000162777 | DENND2D
Description
DENN domain containing 2D [Source:HGNC Symbol;Acc:HGNC:26192]
Coordinates
chr1:111192140-111194726:-
Coord C1 exon
chr1:111194578-111194726
Coord A exon
chr1:111192318-111194577
Coord C2 exon
chr1:111192140-111192317
Length
2260 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGC
5' ss Score
8.07
3' ss Seq
TCCTCTGTGCTCTGTCCCAGCAC
3' ss Score
8.07
Exon sequences
Seq C1 exon
TTCATTTCACTGACACGGCCCCTGGACTCCCACCTAGAACATGTGGATTTTAGTTCTCTATTGCACTGTCTCAGTTTTGAACAGATACTTCAGATCTTTGCCTCTGCCGTGCTGGAGAGAAAAATCATCTTCCTGGCGGAAGGTCTCAG
Seq A exon
GTGGGCCCAGCCCCTGGACGGCTCACCTGAACTGCCCAGCATCCCTGGGTTCAAGGGAACAGACTGGAGGTTATCCAAGGAAAATGGGCTGTAGGGTCCATGCGCCCACCCTCCTGTTTCTAGCTCCTTGTTCTTTAAACCAAGAGAAACAGCTGTTTTGAACCACCCCCACTGCCTCTTCCTCCACACAGGACTGCTGCCTGGGCCTGAGGAATGCTCCTGACTTAGCTTGGGGAAGGACAGGAAGTATTCCTGGGACAGCCTGGGTGGGACCAGTTAGGGTGGATGCAGACATGATTCTGCCCTTGCAAGGCTGAGGGAGGGTGGAGAACAGGGCAGGAGGTAGATACTCATTCAACAAACATTTATTGTGTGTCAACTGGTTGCCAGATGCCAAGCATTGGGAAGATACAAACAGGACAAGGTCCTTCACCTGAAGGGGATGCGGAATTACATACTGGTTGAAAGCACAGGGATTGAAATCAGCAGAATTAGGAGGTTTAAATCCAGTTCTTCTACCTTTAGCTATGAGGTTCCCATTAAGTTAGTTTGTTAACTTCTTAAAAATGGAAATAATGATTGTGATTACCTCATAAGGTTGTGGTGAGGATTAAATGAAATAATGCACATTAGGTACCTAACACCCTGCTGAGCACATATTGCTGAGTGCTAGCTTCTGTTCTTAAGTTCACAGTTGAGTATATCCCTGTGTATAGTGGAAGCAGGGTACTATTGTGCCATGGTCTCTACCTTTTAGGGGCTTCAGATCTGAGAAGGACGTGGGGAGATGTAATAGAATGGAGAATGAAAGAAGTCATAAAACAGTAGGGGTAGGGGTAGACCTTCTATTCATATCTGGGGAGGGAGAAAACCAGTGATTTTAGGTTGACAACCCTGCTTTTATCTTTTAGGGAAGAAGAAAAGGATGTTAGGGACTCAACAGAAGTCAGAGGGGCAGGTGAATGCCATGGGTTTCAGAGGAAAGGAAACTTGGGCAAGCAGTGGGGTCTCTGTGTTGAAGATTCTGTAAAAATGGGTGATAACCAAAGAGGAACTAGTTGTAGGTAATCCTTGAAGGGAGTGGCATCATCTTTTGCTTTGGAAATAGCTCTTTCACTCCCAGCCTTGAATGGAAACCAGAAATTCCTGTGTGGCTAGAGCTGGGATTCTGCCTTTCCTCCTCAGATCAGTGTTTGGGAAGTGGAGGTCGGCAGGATTCACCTCTCAGACGTTTACTTTCTTCAGGGAAATCCCACCACTCCCCACTTCCTTCCCACACTGAGTTTTTCAGCTCCCTGAAGCTCGGACAGGGAGGGGACTTCCAGTCAGCTAGCCTCTCAGAGACTCAATTTTGCTAATTCAGGAAGTGCCAGCTTGAAACCCAGAACTGAAACAAGGATTCCCGCATCTGTGCTTTTATTGGCCTTGACTTTGAGGCAATTTGGCTGGAGTAAAGAAGAGCCATGAAAGCCAGGGGATAAAAGAGAAAGACAGAGAGTGGGACTGTGTGTATGTGGTGGCGAGAGGAGTAGGGTCCAAGTTGTGACTTGGGCAGGAGTGACGAGAAATGCTTCACTGGAAAGTCTTGAGGAGGCACCTTTGTGGGACTTTCCGTGTAGGAATTGCTGGGCAGAGGTTCCTAGAACCTGGGAATTTCCCAAGCTACTCAGGCAGCAACCTGGTAATCTTTAATAACCTCGAGTGTGCCCAGAGGGGGCTGTGTGGGGGCAAAGGCTGGGGATGAGGGTGGATAGACATAGCGAGGTAAAAAGGCTTTGCCTCTCGGCTGAGCCTCCAGTGCTTGTTTACATGTTTGTCTCTTAACTACACTGTGAATTCCTTAAAAGCAGGGTCAGTGTCTTACTCTTCCTGGTATCCACATCTGTGAGGTATGCTCACAGTTGTGAGCACAGGCTAGGGGCTCAATCAATTATCTCCTTGAATGAAAGCAACTCTTCTTCCCTCTTCTCTTCAGAGTCACTTTTATTTTTGGCCAGTAGTAAGTTGAGAAGACTAACTGGGAAAAGAAGGGTCAAATCAAGGCCCTTCTTGATAGTGAAGCCTCAGACTCTCTAGTTTCTGTCCCTCCCTCCCAGCAATGTACGTTCAAGCTCTGTGACCAGCATGGCCCCCAGACTTGCCTTTCTGCCCATGGGCATGGGCAGCACTGCTCTAGCTGCTGTTGGTGGTGGGCGATGAGGGGTGTGTAGCATGGTGGTGCAGGGGCCCCCTGACTCTCATCCTCTGTGCTCTGTCCCAG
Seq C2 exon
CACCTTGTCTCAGTGCATCCATGCTGCTGCCGCACTGCTCTACCCCTTCAGCTGGGCGCACACCTACATCCCTGTTGTCCCTGAGAGCCTTCTGGCCACCGTCTGCTGCCCCACCCCCTTCATGGTTGGAGTACAAATGCGCTTCCAGCAGGAGGTCATGGACAGCCCTATGGAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162777:ENST00000369752:7
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=0.004
Domain overlap (PFAM):
C1:
PF0214116=DENN=FE(26.5=100)
A:
NA
C2:
PF0214116=DENN=FE(31.9=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
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