Special

HsaINT1026506 @ hg38

Intron Retention

Gene
Description
phosphodiesterase 6C [Source:HGNC Symbol;Acc:HGNC:8787]
Coordinates
chr10:93662560-93663178:+
Coord C1 exon
chr10:93662560-93662643
Coord A exon
chr10:93662644-93663027
Coord C2 exon
chr10:93663028-93663178
Length
384 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGT
5' ss Score
11
3' ss Seq
TGACCTAAAATTCCTTTTAGGAG
3' ss Score
7.2
Exon sequences
Seq C1 exon
CCTATGATGGACAGAAACAAAAGAGATGAATTACCTAAACTTCAAGTTGGATTTATTGATTTTGTTTGTACTTTTGTATATAAG
Seq A exon
GTAAGTAAGCAAATTATTTGAATTAAATACATAAACATTTGGATGAGAAATTTTCTTTCAAACTGTCACCAAAATTTAGAAGTCACCCATACGGAAAGCCATTGGGGTATCACTGTTTCTCCAAAGCAGTTTGAGGTTTTACCCTAATCTCATTCAGGGCTGGAATAAAAGGAGGGAACTCAGATGTGAGCGAACTGAACACTTCCTTAGGCAGGCAGTAAAGACAGCACGTGTCTCTTTCCCAAACTTCATAGGCCCGTGGTTAAACTTATCCTAGCAGCTCTGAGTGCTGTAACAATTCCTTACAGCTCACTCTCTGCATATGAAAGATCCTGAAAATTAACTGTATGATTTATGTAGTTTCTGACCTAAAATTCCTTTTAG
Seq C2 exon
GAGTTCTCACGGTTTCACAAAGAAATCACACCTATGCTGAGTGGTCTTCAGAATAACAGAGTAGAATGGAAATCACTAGCTGATGAGTATGATGCAAAGATGAAGGTCATTGAAGAGGAGGCAAAAAAGCAAGAAGGAGGAGCCGAAAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000095464:ENST00000371447:20
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.214 A=NA C2=0.275
Domain overlap (PFAM):

C1:
PF0023314=PDEase_I=FE(10.8=100)
A:
NA
C2:
PF0023314=PDEase_I=PD(7.6=37.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CCTATGATGGACAGAAACAAAAGAGA
R:
TTTTCGGCTCCTCCTTCTTGC
Band lengths:
233-617
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains