Special

HsaINT0117086 @ hg19

Intron Retention

Gene
ENSG00000126883 | NUP214
Description
nucleoporin 214kDa [Source:HGNC Symbol;Acc:8064]
Coordinates
chr9:134039257-134039531:+
Coord C1 exon
chr9:134039257-134039342
Coord A exon
chr9:134039343-134039447
Coord C2 exon
chr9:134039448-134039531
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-NUP214:NM_005085:20
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.257 A=NA C2=0.709
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
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