Special

HsaINT0037725 @ hg38

Intron Retention

Gene
Description
negative elongation factor complex member B [Source:HGNC Symbol;Acc:HGNC:24324]
Coordinates
chr9:137264245-137265979:+
Coord C1 exon
chr9:137264245-137264357
Coord A exon
chr9:137264358-137265876
Coord C2 exon
chr9:137265877-137265979
Length
1519 bp
Sequences
Splice sites
5' ss Seq
GGGGTGAGG
5' ss Score
5.5
3' ss Seq
CCAGGGCGGCCTCCTTCCAGGGA
3' ss Score
6.14
Exon sequences
Seq C1 exon
TTCACCTGGTGCCTGGACGCCTGCATCCGAGAGCGGTTCGTGGACAGCAAGAGGGCGCGGGAGCTGCAGGGGTTTCTCGATGGCGTCAAGAAGGGCCAGGAGCAGGTGCTGGG
Seq A exon
GTGAGGGTCGGCTCCACGAGGCCTCTGCCCCTCAGGGCCCTGCGTGCATCCGGTCTGCGCTTGCTGTGTTTTGCCGTGGGTAGCAGGCGTTTATTCCCGGATATTGCTTTTTCTTTTGTTTTTTTCGAGACAGAGTCTCGTTCTGTAGCCCAGGATGGAGTGCAGTGGTGCAATCTCTGCTCACTGCAACCTCCGCCTCCTAGGCTTAAGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACGCGCCACTGCGCTCAGGTAATTTTTGTATTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTTGTCTTGAACTCCTGACCTCAGGTGATCCACCCGCCTCAGCCTTCCAAAGTGCTGGGATTACAGGCATGCGCCACCGTGCCTGGCCTCCTGGATGTTTCAATAGAGCTATGCCGGGCACTGCTGGCCCACAGCTTAGGGACATGGTTGTCGGGATGTGTGTGGGTAGCAAAGTCTCCCTCCTCAACTCTGCATTCTGGAGCCAGGCCCAGGGGCTGGGGTCTGGTGTCTGCAGTGGCGTGGGGTCAGCCTCTGAGCTGAGGGGCATCCATTGGCATTTGCTTTCCAGCATCCTCTGGCTGGTGTATAGACACAGTGCTGCCTGGCCCTGCCTTTGCCACTTTTTTTCTTCCTTTTTTTTTTTTTTTTTTTTTTTCTGAGACAGGGTCTCTGTCACCCAGGCTTTAGTGCAGTGGTACAGTCTCCCTCAACCTCCTGGGCATTGATCCTGCTGTCTCCGCCTCCCAAAGTGCTGGGATTACAGGCACACACCAGTGCGCCTGGCCGATTTTTGTTATCTTTAGTAGAGATGGGATTTCACCACCTCGCCCGGGCTAGTCTCAAACAAACAATCCACCGGCCTCAGCATCCCAAAGTGCTGGGATGACAGGCGTGAGCCACCACACCCAGCCTTTTTTTTGTTTGTTTTTTTAACTTTTTAATTTGAAAAATCTTTGAATAGGTTAAGGACAAATTGCAAACCTTAAGCTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTCTTGCCCAGGCTGGAGTGCAGTGACGCGATCCTGGCTCACTGCAAGCTCTGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACCACAGGCGACCACCACCACGCCCGGCTAATTTTTTGTATTTTTGGTAGAGACAGGGTTTCACTTTGTTAGCCAGGCTGGTCTCAGTCTCCTGACCTGGTGATCCATCCGCCTCGGCCTGCCAAAGTGCTGGGATGACAGGCTGAGCCGCCGCGCCCGGCCTGCCAAAGTGCTGGGATGACAGGCTGAGCCGCCGCGCTCGGCCATCCTTAAGCTTTTTGTAAGAAACCCAGCATGTGATGGGCACCCGCTGCCAGTCCTGAATTCAGCCTAGGCCACCCCTCCTGAGGACTGTGCCGCTGAAGGGAGGGGCAACAGGCGTCGCATTAATGCCAGGGCGGCCTCCTTCCAG
Seq C2 exon
GGACCTGTCCATGATCCTGTGTGACCCCTTCGCCATCAACACGCTGGCACTGAGCACAGTCAGGCACCTGCAGGAGCTGGTCGGCCAGGAGACACTGCCCAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000188986:ENST00000343053:6
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:
PF062098=COBRA1=FE(7.8=100)
A:
NA
C2:
PF062098=COBRA1=FE(7.2=100)


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:
TTCACCTGGTGCCTGGACG
R:
CCTGGGCAGTGTCTCCTGG
Band lengths:
216-1735
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