Special

HsaINT0122173 @ hg38

Intron Retention

Gene
Description
phosphodiesterase 6B [Source:HGNC Symbol;Acc:HGNC:8786]
Coordinates
chr4:664881-665329:+
Coord C1 exon
chr4:664881-664944
Coord A exon
chr4:664945-665254
Coord C2 exon
chr4:665255-665329
Length
310 bp
Sequences
Splice sites
5' ss Seq
AAGGTTAGA
5' ss Score
6.12
3' ss Seq
CTGCCTTCCTGTGCCTCCAGGTC
3' ss Score
11.96
Exon sequences
Seq C1 exon
GGCCATGATGATGACAGCCTGCGACCTGTCTGCCATCACCAAGCCCTGGGAAGTCCAGAGCAAG
Seq A exon
GTTAGAACAGAGGGCCCTCCAGACCCAGAGTCAGTGCCTCTCAGCACATGGGACTGCCGGGCGGGCGGGAGCCTCGGATGGCAACGGACCATTGTTTGCAAGGAGCTCTGAGGGCCACCTCGGGGCCAGGCCAGGGCGGCAAGGATGGGGGTACTGCAGTGTGTCTACATGGCTCAACCGGAGCCCTGTGTGGTGGGGACCCCGGGGGTCTGGGGCGGAGAAGACCGAGGCTCGGAGCCTCACGGGGCGGGCCCGGGCCCTTCCGCGTGGGCTCAGAGCTCCACAGACAGCTGCCTTCCTGTGCCTCCAG
Seq C2 exon
GTCGCACTTCTCGTGGCTGCTGAGTTCTGGGAGCAAGGTGACTTGGAAAGGACAGTCTTGGATCAGCAGCCCATT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000133256:ENST00000255622:18
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.032
Domain overlap (PFAM):

C1:
PF0023314=PDEase_I=FE(14.6=100)
A:
NA
C2:
PF0023314=PDEase_I=FE(29.4=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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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