HsaINT0116936 @ hg38
Intron Retention
Gene
ENSG00000095319 | NUP188
Description
nucleoporin 188 [Source:HGNC Symbol;Acc:HGNC:17859]
Coordinates
chr9:128999172-128999805:+
Coord C1 exon
chr9:128999172-128999317
Coord A exon
chr9:128999318-128999623
Coord C2 exon
chr9:128999624-128999805
Length
306 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
3' ss Seq
CCTCCCTGTCTATTCTACAGTAA
3' ss Score
7.33
Exon sequences
Seq C1 exon
AGAGTTAGGTTCTGTGGATGAAATCCTTGGACCCTTGACGGAGATCCTGGAGGGAGTGCTGCAGGCCGACCAGCAACTCATGGAGAAGACCAAGGCCAAGGTGTTCTCAGCATTCATCACAGTGTTGCAAATGAAGGAGATGAAAG
Seq A exon
GTGAGGGGCAGAGGCAGGGGGAGCAGCAGCTGCAGTCTGCCCACTCCTGCTGACAGCCAGGCAGGGCTTCCTTCAGCTTAGGGCCACACATTTCTTCTGGGACTTTTGAGTTTCCAGTCATGGAATTCTTACCCCAAGAAAGCTATTTTTTTCCCTCATGTGTCTCTCCCTCCTCTCCCACTGGACAGATGCTGTCCCTCCTAGCGCCCTAGTACATCTCCAGCCCCTTCCTAGGAAGGAAACCTTGGTGTACAGTGAGAGTTGGCCTGGTGAGCATGACAGTGTCCCTCCCTGTCTATTCTACAG
Seq C2 exon
TAAGTGACATCCCCCAGTACTCCCAGCTGGTGCTGAATGTCTGTGAGACCCTCCAAGAGGAAGTGATTGCACTCTTCGACCAGACCCGCCACAGTCTGGCATTAGGCAGTGCCACAGAGGACAAGGACAGCATGGAGACTGACGACTGTTCTCGGTCCCGGCACAGGGACCAGCGTGATGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000095319:ENST00000372577:33
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=0.213
Domain overlap (PFAM):
C1:
NO
A:
NA
C2:
NO
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
AGAGTTAGGTTCTGTGGATGAAA
R:
CATCACGCTGGTCCCTGTG
Band lengths:
326-632
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