Special

HsaINT0132653 @ hg38

Intron Retention

Gene
ENSG00000110844 | PRPF40B
Description
pre-mRNA processing factor 40 homolog B [Source:HGNC Symbol;Acc:HGNC:25031]
Coordinates
chr12:49631401-49631925:+
Coord C1 exon
chr12:49631401-49631544
Coord A exon
chr12:49631545-49631859
Coord C2 exon
chr12:49631860-49631925
Length
315 bp
Sequences
Splice sites
5' ss Seq
CAGGTAATT
5' ss Score
8.55
3' ss Seq
TGTCTTCTTTGTATCCATAGATA
3' ss Score
10.68
Exon sequences
Seq C1 exon
ATGCCCCCTCCAGGGATCCCCCCACCCTTTCCTCCGATGGGGCTACCCCCCATGAGTCAGAGACCACCAGCTATCCCCCCCATGCCACCTGGCATCCTGCCCCCAATGCTTCCACCAATGGGGGCGCCACCACCACTCACACAG
Seq A exon
GTAATTGTCTCTCCTCCCCTGGGGCCTCAGAAAACCCTGTCAGTTTAGCTGGGGGTGGAGATAAGAGCGGGCATGTAGGCCTCAGAAACTGGGGAAGGAAGGGAGCTTTGGGCCAAACCCATGTGGATTTGTCTGCTGAATGACTGAGACAACTCTCAGGCAAGGTGAGAGGCCAGAATCTGGGGATTGCCTGAGGAAGTGCCCAAGTGAGGGTCATGGCTCCAGTGAGATGTCTCAGGACCCTTTGAGGTACCCTGTCCCTCCTGTTCCAGCCCTTACCTTGGTGGTTGGTTTCTGTCTTCTTTGTATCCATAG
Seq C2 exon
ATACCAGGAATGGTACCTCCGATGATGCCAGGAATGCTGATGCCAGCGGTGCCTGTCACCGCAGCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000110844:ENST00000380281:2
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.993 A=NA C2=0.485
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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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