HsaINT0116916 @ hg19
Intron Retention
Gene
ENSG00000095319 | NUP188
Description
nucleoporin 188kDa [Source:HGNC Symbol;Acc:17859]
Coordinates
chr9:131743543-131744980:+
Coord C1 exon
chr9:131743543-131743669
Coord A exon
chr9:131743670-131744827
Coord C2 exon
chr9:131744828-131744980
Length
1158 bp
Sequences
Splice sites
5' ss Seq
TTGGTGAGA
5' ss Score
6.29
3' ss Seq
AATTTATCTTTCTCTCTCAGGGG
3' ss Score
9.85
Exon sequences
Seq C1 exon
GTGTATAGCTTCTTGGATAAGATGTCTTTCTACAATGAACTTTATAAACACAAGCCTCATGATGTGATCTCCCATGAAGATGGAACTCTTTGGCGGAGACAAACACCCAAACTCCTTTATCCCCTTG
Seq A exon
GTGAGATAAAGAGATCCCCCTTTTATGACAGCTTTTTTTTTTTTTGATGTCTTGCTCTGTCACCCAAGCTGGAGTGCAGTGGCAAGATCATAGCTCACTGCAGCCTCAAATTCTTGGGCTCAAGTGATTCTCCCACCTTAGCCTCCCAAAGCACTGGGATTATAGACGTGAGCCAATGCATCCAGGCAGTTACACTCTGAGGCTCACATCTGTACCAGGTGCTCAAAGAGGAAAATATACAGGGAATAGCCTCACCGTTTTAATCCTGGCATCATCACCACTGACTTCTCCAGTCATCTAGGCACTAACAGTCCTATGAGGTACTGTTGTTATCATCATTTGAATGGAAAACTGTTCTTTGCACTCAAGTGATTTTCAGACATATAGAAAGAGTCACTTGTCGGCCAGGTGTAGTGGCTCACGCCTGTAATCCCAACACTGGGATTACAGGCCAAGGTGGGCGGATCACGTGAGGTCGGGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATATAAAATTAGTCGGGCGTGGTGGTGCATGCCTGTAATCCCAGCTACTCGGGAGGCTAAGACAGGAGAATCGTTTGAACTTGGGAGGCAGAGGTTGCAGTGAGTTGAGATCGCGCCATTGCACTCCAGCCTGGGCAGCAAGAGCAAAACTCCATCTCAAAAAAAAAAAGACACTTGTCTACATGACAAGAACTTTTTTGTGTATTTTAGTTGAAAAAGCTTTAGGAATGTTAGCTACTAAGAAGAAAGCCTGTGAATCCCAGAACTTTGGGAGGCCAAGACAGGCAAATCACTTGAAGCCAGGAGCTCAAGACCAGCCTGGTCAACATGGAAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGAGTGGTGGTGCGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAAGCACGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGCGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCAAGAGGGAGACTCTGTCTCAAAAAAAAAAAATGTCTGTGAGTTTGTGTATCTCTGTGTGTTTAAAATATTGATGTCTGGTAGAGGAGTTACATTTTTTATTTATCCTCAGATATTAGACTAATTTATCTTTCTCTCTCAG
Seq C2 exon
GGGGTCAAACCAACCTTCGCATACCTCAAGGCACTGTGGGCCAAGTAATGTTGGATGATAGGGCATACCTGGTACGCTGGGAATACTCCTATAGCAGCTGGACCCTCTTTACCTGCGAGATTGAAATGTTGCTTCATGTTGTTTCAACTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000095319-NUP188:NM_015354:15
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:
PF104874=Nup188=FE(4.6=100)
A:
NA
C2:
PF104874=Nup188=FE(5.6=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:
TGTATAGCTTCTTGGATAAGATGTCT
R:
TGCAGTTGAAACAACATGAAGCA
Band lengths:
278-1436
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
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)