Special

HsaINT0048120 @ hg19

Intron Retention

Gene
Description
DIP2 disco-interacting protein 2 homolog B (Drosophila) [Source:HGNC Symbol;Acc:29284]
Coordinates
chr12:51090844-51092250:+
Coord C1 exon
chr12:51090844-51090958
Coord A exon
chr12:51090959-51092110
Coord C2 exon
chr12:51092111-51092250
Length
1152 bp
Sequences
Splice sites
5' ss Seq
CAGGTACTG
5' ss Score
9.04
3' ss Seq
TGATGGGTTCTTCTTTTCAGGCC
3' ss Score
9.46
Exon sequences
Seq C1 exon
GGTCCGTGTCATCCTGTGATGCCTTCCTGAGTCTGTTCCAAAGTCATGGACTGAAGCCTGAGGCCATCTGTCCGTGCGCCACGTCTGCTGAAGCCATGACTGTAGCAATCCGCAG
Seq A exon
GTACTGTTCAGGATGTCAGATGCTCTTGATGTATGTTACAACTTGGATGAAATGTGCAGTATTTACCAGGTGATGACCAACGGATGTTAACTAATTTTCTAAGCAGTTTCAAGCATCTCATTTTTCCCACTCTTGCTCAAAGTGTATGCAGTAAACTGAAAAATTTAATTGATATCATTTCGTATTTGTGAATTAGCTCTTTTTCTGTGCCATTTTGCTCTTCGGAATCCATAGCACCTTAGATTAAAAATAGACTGTTCTTGATTGTAGCTTAAGTATGGATAGTATATCTATAGTATATTCAAGACCATTATGTATGTAAGTATCAGTGAATGTGTGTGTGTGTATATAGATATACTTTTTTTTTTTTTTTTTTTTTTTTTTTAGATAGGATCTCTCTTTGTCACCCAGTGGCATGATTATGGCTCACTGCAGCCTCAACCTCCTGGGCTCAAACAGTCCTCCTGCCTCAACTTCCTGAGTAGCTAGGACTACAGGCATGTACCACCACGCCTGGCTAATTTTTAAATTTTTTTGTAGAGATAGGTTCTTGTTATGTTGCCCAGGCTGGTCTCGAATTACTGGCTTTGAGCAGTCCACCTTCCTTGTCCTCCCAAGTGCTGGGATTGTAAGCATGAGCCACCAAGCCTGGCCCAGTACGCAATACTTGATGATGATGATAAATGACCATTTTGCTGGTTTATGTGTTTACTACACTACATTTTTTTTAAATTTAATTTTTGAGAGATGGGGTCTTGCTCTGTTATCCAGGCTGGAGCACAGTGACACGATCATTGTAGCCTCAACCTCCCAGGCTCAGATGGTTCTCCCACCTTAGCCTCCCAAGTAGCTGGGACTACAAGCATGTGCCATCATACCCAGCTAATTTTTGTATTTTTTGTAGAGATGGGGGTCCCACTGTGTTGCCCAGGCTGGTTTTGAACTCCTGGCCTCAAGCAATCCTCCTGCCACAGCAGTTGCTGGGATCACAGGTGTGAGACACCACACCCAGCTCTAATTTGGCATATTTTTGGGAGAGAAAATGGAGAATTTTTTTGGTATTGTAGCCAGAGGAAATTTGTCTTCCTATGTATTTGTATTTTTCCCTTGATGTTATTTCATTCACCAAACTTGATGGGTTCTTCTTTTCAG
Seq C2 exon
GCCTGGAGTTCCAGGAGCCCCTTTGCCAGGAAGAGCCATTCTCTCAATGAATGGATTGAGCTATGGGGTAATACGGGTCAATACTGAAGATAAAAATTCAGCACTGACGGTCCAGGATGTAGGGCATGTAATGCCTGGTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000066084-DIP2B:NM_173602:17
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=0.021
Domain overlap (PFAM):

C1:
PF0050123=AMP-binding=FE(8.0=100)
A:
NA
C2:
PF0050123=AMP-binding=FE(9.9=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GTCCGTGTCATCCTGTGATGC
R:
CATTACATGCCCTACATCCTGGAC
Band lengths:
247-1399
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development