Special

HsaINT0132655 @ hg19

Intron Retention

Gene
ENSG00000110844 | PRPF40B
Description
PRP40 pre-mRNA processing factor 40 homolog B (S. cerevisiae) [Source:HGNC Symbol;Acc:25031]
Coordinates
chr12:50036710-50037180:+
Coord C1 exon
chr12:50036710-50036799
Coord A exon
chr12:50036800-50037005
Coord C2 exon
chr12:50037006-50037180
Length
206 bp
Sequences
Splice sites
5' ss Seq
TCAGTGAGT
5' ss Score
7.68
3' ss Seq
GTATCTGCTGATCTGCCCAGGGC
3' ss Score
5.38
Exon sequences
Seq C1 exon
CAGACTGAATGCCAGCACCTCCACACCAAAGGCCGAAAGCATGGCAGGAAAGGCAAGAAGCACCATCACAAGCGTTCCCACTCACCCTCA
Seq A exon
GTGAGTAAGCGTGTAGAAGGGACATGGGGTGAAGCTGGGTTGTTTTGGGGAAATAAACACTTTGTTTTCCCCTTACAATATCTCCCTTGGAGGGAAGTTTGAGGATTCCTTTGGCCCTGGGTCCTCCTCCTCTCTCGAATTCCCAGACGAGGGCTTCTGGAGGGCAGAGAACCTCTGCACTGACATGTATCTGCTGATCTGCCCAG
Seq C2 exon
GGCTCTGAGTCAGAAGAAGAGGAGCTGCCCCCACCATCTCTCCGGCCCCCCAAGCGGAGGAGGCGGAACCCCTCAGAGTCAGGCTCTGAGCCCTCTTCCTCACTTGATTCAGTTGAAAGTGGGGGTGCTGCCCTTGGAGGACGGGGCTCCCCTTCCTCCCATCTTCTTGGAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000110844-PRPF40B:NM_001031698:21
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.933 A=NA C2=1.000
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:
CAGACTGAATGCCAGCACCTC
R:
TGCTCCAAGAAGATGGGAGGA
Band lengths:
264-470
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