Special

HsaINT0124972 @ hg19

Intron Retention

Gene
ENSG00000133056 | PIK3C2B
Description
phosphoinositide-3-kinase, class 2, beta polypeptide [Source:HGNC Symbol;Acc:8972]
Coordinates
chr1:204433140-204433732:-
Coord C1 exon
chr1:204433578-204433732
Coord A exon
chr1:204433261-204433577
Coord C2 exon
chr1:204433140-204433260
Length
317 bp
Sequences
Splice sites
5' ss Seq
ACTGTAAGT
5' ss Score
8.59
3' ss Seq
CCCTACCTTACCCTTCACAGGTT
3' ss Score
8.79
Exon sequences
Seq C1 exon
CCTTCGATCTGGCTCTGACATCCAAGACTACTTCCTCACTGGCTATGTCTGGAGTGCTGTCACCCCTAGCCCAGAGCACCTCGGGGATGAGGTCAACCTGAAGGTGACTGTGTTGTGTGACAGGCTTCAAGAGGCACTCACTTTCACCTGCAACT
Seq A exon
GTAAGTTAGTGAGGGGGGAGAGGATGTGAGCATCCCTTGAAGTGGGGTGGGGATGACTGTGTTTTGACTCGATTTCCACCTCATCTTGTGGCCCAGATGAAGGGCAGTGAGGATGCTCCTTTGGGGGTGAGGGGCTGGCTATGGGGCCAGCATTCTAGTACAGTCACTTTCCTCAACTCTGAACTACTTGCCTGCTTTATCTGGTTGGTGATGGTGCTGGAGAATACTTAGCTGGAAAGGGGGATCAGGGTGGGGAAACTGAGACCCATCTGCCTTGACATCCATCATGATTGCTCCCCCTACCTTACCCTTCACAG
Seq C2 exon
GTTCCTCCACTGTAGACTTGCTTATCTACCAGACCCTGTGCTACACCCATGATGACCTGAGGAATGTGGACGTGGGTGACTTTGTGCTAAAGCCCTGCGGGCTGGAGGAGTTCCTGCAGAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000133056-PIK3C2B:NM_002646:5
Average complexity
IR-S
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:
PF0079413=PI3K_rbd=PU(32.0=62.3)
A:
NA
C2:
PF0079413=PI3K_rbd=FE(38.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCGATCTGGCTCTGACATCCA
R:
GAACTCCTCCAGCCCGCAG
Band lengths:
265-582
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