Special

HsaINT0132645 @ hg38

Intron Retention

Gene
ENSG00000110844 | PRPF40B
Description
pre-mRNA processing factor 40 homolog B [Source:HGNC Symbol;Acc:HGNC:25031]
Coordinates
chr12:49634332-49634602:+
Coord C1 exon
chr12:49634332-49634455
Coord A exon
chr12:49634456-49634537
Coord C2 exon
chr12:49634538-49634602
Length
82 bp
Sequences
Splice sites
5' ss Seq
AAGGTGCTG
5' ss Score
4.05
3' ss Seq
TCCCACCTGCTTCATTCCAGGCT
3' ss Score
7.7
Exon sequences
Seq C1 exon
TTCTGGACAGCATCAGCCACAGCAGGAGGAGGAGGAATCAAAGCCAGAACCAGAGAGGTCTGGCCTCAGTTGGAGCAACCGGGAGAAGGCAAAGCAGGCATTCAAGGAACTGCTGAGGGACAAG
Seq A exon
GTGCTGGAGTGGGGCTCCCAGGGAAGGTTTGGAGGGGGCTGGAGCGGGGCAGGCCCCATGACTCCCACCTGCTTCATTCCAG
Seq C2 exon
GCTGTCCCCTCCAATGCCTCATGGGAACAGGCCATGAAGATGGTGGTCACCGACCCCCGTTACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000110844:ENST00000380281:10
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=NA C2=0.909
Domain overlap (PFAM):

C1:
PF0394210=DTW=FE(35.7=100),PF0184614=FF=PU(24.0=28.6)
A:
NA
C2:
PF0394210=DTW=FE(18.3=100),PF0184614=FF=FE(42.0=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:
TTCTGGACAGCATCAGCCACA
R:
CCATCTTCATGGCCTGTTCCC
Band lengths:
167-249
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development