HsaINT0116937 @ hg19
Intron Retention
Gene
ENSG00000095319 | NUP188
Description
nucleoporin 188kDa [Source:HGNC Symbol;Acc:17859]
Coordinates
chr9:131761903-131764008:+
Coord C1 exon
chr9:131761903-131762084
Coord A exon
chr9:131762085-131763807
Coord C2 exon
chr9:131763808-131764008
Length
1723 bp
Sequences
Splice sites
5' ss Seq
GGGGTGAGA
5' ss Score
4.74
3' ss Seq
TCATCTTTGCCTCTGGGCAGGTG
3' ss Score
10.03
Exon sequences
Seq C1 exon
TAAGTGACATCCCCCAGTACTCCCAGCTGGTGCTGAATGTCTGTGAGACCCTCCAAGAGGAAGTGATTGCACTCTTCGACCAGACCCGCCACAGTCTGGCATTAGGCAGTGCCACAGAGGACAAGGACAGCATGGAGACTGACGACTGTTCTCGGTCCCGGCACAGGGACCAGCGTGATGGG
Seq A exon
GTGAGACAGTGCCCTAGAAGGCCATCCGTCCTTTCCACTGCCCGCCAGCTCTGTGCCTGACTCTGGGGATAAGTAGTGATCAAGACAGATAGTCGCTGCACTTCTGGAGTTCACGGCCTGGTGGGAAAGGTTAATAGATCAGACACTGCAGAAAAGCAGAAGCAGCCCATTGTACTGCAGGAGAGAAGTGCAGGGAGAACTTAGTCTCACTTCTGACTTGAACTGGGACTTAGGTGCCTTTTCAGCAATGACTTAGAGATTGTAGCCGCGGGCAAATGCAGGATCCGAAGTGAAATAGGAAATGATGTAAGGCTTTTAAGCAGGGGAAAAAGTTGATCTGATTTTTACTCTAGAAAGATCACTCTGGACTTAAACTCCAGGCCTCAAGCCATCCTCCCAGTTCAGCCTTCCAAAGTGTTGGGATTACAGGCGTGCCCAAGAAAGATCACTCTGGATGCAGTATTGAATAGTATTTTTCAAATTGTGGGATCATGACCTATTAGAGAGAGTCTTGAAATTAGCACATTTTGTTACAACCAGTCTCGCTCTGTCGCCCAGGGTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAAGCTCTGCTTCCCAGATTCACGCCATTCTCCCACCTCAGCCACCCGAGTAGCTGGGGCTACAGGTGTCTGCCACCACGCCCGGCTAACTTTTTGTATTTTTCATAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGCCTCGATCTCCTGACCTCGTAATCCGCCCGCCTTGATCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCTGGCCACAACCAGCATTTTTTTAAAATAAAGTAGAATAAAGTGTTTAAGAAAATATCACTGTGCTTTGTGTGACATTAGGGTAGGTATTATTAGTGAAAAACTGTAAACGTGTACATGAGGATACAGTCTAAAAAGTCTTTATGGGCCGGGCACGGTGGCTAACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGATCATGAGGTCAGGAGATGGAGACCATCCTGGCTAACACGGTGAAACCCTGTCTCTATGAAAAATACAAAAAATTAGCCGGGCGTGGTGGCGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGGATGGCGTGAACCCAGGAGCGGAGGTTGCAGTGAGCCGAGATCGCGCCGCTGCACTCCAGCCTGGGGGACAGAGCGAGGCTCCATCTCAAAAAAAATGTCTTTATGACTCTGGGTCATGGCCAAAAAGAAGGTTGAAAGGCCACTGGTACAAGGATAGATTAGAGAGGATGGAGCAGGATTATTTAGGAGATGGTTGCAGTAGCAGAGCAGGAGGTGGCATCGGGCAGGGTCGTAGGGGTCCCTCAGACTCCATGTGGCAGAGTTGGTTGGAGTGTCCAACATGAGACGAGGTGGCTCTGACAAGGGTGGTGGCAGTGTGGGAGGTGGGAGGGAAGAGGCGGGGGTAGCTCTGGTCAGTTTAGGGTTGCTCATTAGATTGGCTGGAGTTGCTGCTGTTCATTGAGAGCTGGACATAGGAGAGGGGCAGGGTGGGAGAGAGTGTGCATTCTGTGTTACTCAAGCTCACTTAGCAATGTGTGTAACCAAGCAGGTCTTGGGCAACCAGGCCCACCGCTGCCTGTCGTCCTCTTCCTCCTCCTCTTCTTCTTCCCCCTTTTACTCATCTTTGCCTCTGGGCAG
Seq C2 exon
GTGTGTGTCCTGGGCCTGCACCTGGCCAAGGAGCTGTGTGAGGTAGACGAGGATGGTGACTCCTGGCTGCAGGTAACCCGCAGGCTCCCCATCCTACCCACCCTCCTCACCACTCTAGAGGTGAGCCTTCGCATGAAGCAGAACCTGCATTTCACTGAGGCCACATTGCATCTGCTCCTCACCCTGGCTCGCACTCAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000095319-NUP188:NM_015354:34
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.213 A=NA C2=0.000
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:
GACATCCCCCAGTACTCCCAG
R:
AGATGCAATGTGGCCTCAGTG
Band lengths:
350-2073
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)