Special

HsaINT0117086 @ hg38

Intron Retention

Gene
ENSG00000126883 | NUP214
Description
nucleoporin 214 [Source:HGNC Symbol;Acc:HGNC:8064]
Coordinates
chr9:131163870-131164144:+
Coord C1 exon
chr9:131163870-131163955
Coord A exon
chr9:131163956-131164060
Coord C2 exon
chr9:131164061-131164144
Length
105 bp
Sequences
Splice sites
5' ss Seq
CAGGTAATT
5' ss Score
8.55
3' ss Seq
GGTTTATGGATTTCTTGCAGCCA
3' ss Score
6.47
Exon sequences
Seq C1 exon
TTTTGACAGTGACCTGGAAAGCCTGTGCAATGCTTTGTTGAAAACCACCATAGAATCTCACACCAAATCCTTGCCCAAAGTACCAG
Seq A exon
GTAATTGCATCCTTCCCAGTCTTTTAACTCCCTTTATTCTCTTCCAAGTACTGATATCTTAAAAACTGAGTCTTAATCATTTATGGGTTTATGGATTTCTTGCAG
Seq C2 exon
CCAAACTGTCCCCCATGAAACAGGCACAACTGAGAAACTTCTTGGCCAAGAGGAAGACCCCACCAGTGAGATCCACTGCTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000126883:ENST00000359428:20
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.267 A=NA C2=0.759
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TTTTGACAGTGACCTGGAAAGCC
R:
CTGGAGCAGTGGATCTCAC
Band lengths:
170-275
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