Special

HsaINT0037721 @ hg38

Intron Retention

Gene
Description
negative elongation factor complex member B [Source:HGNC Symbol;Acc:HGNC:24324]
Coordinates
chr9:137255907-137256428:+
Coord C1 exon
chr9:137255907-137256070
Coord A exon
chr9:137256071-137256328
Coord C2 exon
chr9:137256329-137256428
Length
258 bp
Sequences
Splice sites
5' ss Seq
AAGGTGGGT
5' ss Score
8.23
3' ss Seq
AATCCTGTGAGTTGTTCCAGGTA
3' ss Score
2.3
Exon sequences
Seq C1 exon
ACAGAGAATGGTGTGCTGCTGCCATCTCTTCAGTCAGCCCTCCCCTTCTTGGACCTGCACGGGACGCCGCGGCTGGAGTTCCACCAGTCGGTATTCGATGAGCTGCGGGACAAGCTGCTGGAGCGAGTGTCAGCCATCGCTTCGGAGGGGAAGGCTGAGGAAAG
Seq A exon
GTGGGTCAGCGGGAGGGGTGGGCAGGTGAGATGTGCAGCCGGCCTCTCAGCCTTGGATCGACTCAGGGGCATTTATTGTCCTTTTGGCTCCACATCCTTGCTCCCAGAGGTGGCCTGGGCCTGTGTCTGAGTGACCCCTTGACCCATGTGTCCTGGGCGTGGAGGCTTGTCCTGGTAGCTGTTATCTGTGTAGGGACAGGCAGGTAGCTGCTGCGATTTGGCGCATCGCTGCACCATCAATCCTGTGAGTTGTTCCAG
Seq C2 exon
GTACAAGAAGCTGGAAGACCTTCTGGAGAAGAGCTTTTCTCTGGTGAAGATGCCGTCCCTGCAGCCCGTGGTGATGTGCGTCATGAAGCACCTGCCCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000188986:ENST00000343053:2
Average complexity
IR
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:
NO
A:
NA
C2:
PF062098=COBRA1=PU(3.4=47.1)


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:
ACAGAGAATGGTGTGCTGCTG
R:
CTTGGGCAGGTGCTTCATGAC
Band lengths:
264-522
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