Special

HsaINT0116936 @ hg19

Intron Retention

Gene
ENSG00000095319 | NUP188
Description
nucleoporin 188kDa [Source:HGNC Symbol;Acc:17859]
Coordinates
chr9:131761451-131762084:+
Coord C1 exon
chr9:131761451-131761596
Coord A exon
chr9:131761597-131761902
Coord C2 exon
chr9:131761903-131762084
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-NUP188:NM_015354:33
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=0.213
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
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