Special

HsaINT0132662 @ hg38

Intron Retention

Gene
ENSG00000110844 | PRPF40B
Description
pre-mRNA processing factor 40 homolog B [Source:HGNC Symbol;Acc:HGNC:25031]
Coordinates
chr12:49633014-49633547:+
Coord C1 exon
chr12:49633014-49633124
Coord A exon
chr12:49633125-49633426
Coord C2 exon
chr12:49633427-49633547
Length
302 bp
Sequences
Splice sites
5' ss Seq
GAGGTCCTG
5' ss Score
-2.13
3' ss Seq
CCTATCCCATCCACTTGCAGCTG
3' ss Score
10.68
Exon sequences
Seq C1 exon
AGGGCCCTATGGAGTGAGCATGTGGCCCCAGATGGGCGCATCTACTACTACAATGCTGACGACAAGCAGTCCGTGTGGGAGAAGCCCAGCGTGCTCAAGTCCAAGGCAGAG
Seq A exon
GTCCTGAGCTGGGCTTTCTGGCCCTTCCTTTCAGCTGCCCTGACCCTTCCAAGTCCTTGGCCTTCCCTTAGTCTCTAACCATATTCATGATGGTTCCTCTGATCCCAAGGTCCCTGACCATTCCTCACCCTCCCTGGAAATGCCTCCATAGGATCTCAAGAAGTCCACCTTCCCCAGTTTGAACCAGGCCAGGTGGTAGCTAAAGGTTCCTGTGTCCTCTACTCACTAGGTCCCCTTAGCTCCCCTGACTGGCTGGAGAACTTGCCCATCCCACTGATGGCTCCTATCCCATCCACTTGCAG
Seq C2 exon
CTGCTCCTGTCCCAATGTCCCTGGAAAGAGTACAAGTCGGACACAGGCAAACCTTATTACTATAACAACCAGAGTAAAGAGTCCCGCTGGACCCGGCCCAAGGATCTGGATGACCTAGAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000110844:ENST00000380281:6
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.387 A=NA C2=0.683
Domain overlap (PFAM):

C1:
PF0039721=WW=PD(90.3=75.7)
A:
NA
C2:
PF0039721=WW=WD(100=73.2)


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:
AGGGCCCTATGGAGTGAGCAT
R:
TCTAGGTCATCCAGATCCTTGGG
Band lengths:
230-532
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