Special

HsaEX6065376 @ hg19

Exon Skipping

Gene
ENSG00000139144 | PIK3C2G
Description
phosphoinositide-3-kinase, class 2, gamma polypeptide [Source:HGNC Symbol;Acc:8973]
Coordinates
chr12:18715637-18719991:+
Coord C1 exon
chr12:18715637-18715826
Coord A exon
chr12:18716311-18716432
Coord C2 exon
chr12:18719883-18719991
Length
122 bp
Sequences
Splice sites
3' ss Seq
TATCTATTTACTTTCTGCAGCTG
3' ss Score
8.48
5' ss Seq
AGAGTAAGG
5' ss Score
5.42
Exon sequences
Seq C1 exon
GAAAATAAAGGAAAGTCTGGAGTGTTTCCCTGTTAAATTGAATAACTTGATCCACACACTTGCACAAATGTCAGCCATAAGCCCTGCCAAATCTACTTCACAGACTTTTCCTCAGGAATCCTGTTTGCTGAGTACAACTAGGTCGATTGAAAGAGCAACAATTTTAGGGTTCAGCAAGAAATCCAGTAAT
Seq A exon
CTGTATCTGATCCAGGTGACACACAGCAACAACGAAACAAGCCTGACAGAAAAATCATTTGAGCAGTTTTCAAAACTTCACAGCCAACTTCAGAAGCAGTTTGCATCACTGACTCTCCCAGA
Seq C2 exon
GTTTCCTCATTGGTGGCACCTACCTTTTACAAATTCAGATCACAGAAGATTCAGAGATCTAAATCATTACATGGAACAGATATTAAATGTATCACATGAAGTTACAAAC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000139144-'26-27,'26-26,27-27=AN
Average complexity
A_S
Mappability confidence:
88%=100=75%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
PF0078719=PX=PU(16.0=26.6)
A:
PF0078719=PX=FE(37.7=100)
C2:
PF0078719=PX=FE(34.0=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
AAGGAAAGTCTGGAGTGTTTCCC
R:
GATCTCTGAATCTTCTGTGATCTGA
Band lengths:
242-364
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains