Special

HsaINT0122183 @ hg38

Intron Retention

Gene
Description
phosphodiesterase 6B [Source:HGNC Symbol;Acc:HGNC:8786]
Coordinates
chr4:656874-657494:+
Coord C1 exon
chr4:656874-657023
Coord A exon
chr4:657024-657350
Coord C2 exon
chr4:657351-657494
Length
327 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAGC
5' ss Score
9.85
3' ss Seq
GACACTGCCATCCCCTCCAGTCC
3' ss Score
7.48
Exon sequences
Seq C1 exon
GAAGGGGCCCTGGACGACTCCGGGTGGCTCATCAAGAATGTGCTGTCCATGCCCATCGTCAACAAGAAGGAGGAGATTGTGGGAGTCGCCACATTTTACAACAGGAAAGACGGGAAGCCCTTTGACGAACAGGACGAGGTTCTCATGGAG
Seq A exon
GTAAGCACCTGGGCAGACGTGGTTCCGCCGGGGATGCCCTGCGAGGGGTGGGGCCTGTGCGGTGTGGGGGCCTCCCCGCCAAGCATTCGGCTGTGTGCGTGTGCTCATGTGTGTGCGGTATGCATGCGGCCAGGGAGAGGACGACAAAGGGCCCCCCCGGGAGCAGGAGCCTCTGCAGAGCACCCGGGAGACCCCACACAGAAGCACTGCGACACCATGGTGGCAGCCCCAGGACCTGCCCGCCGAGCCACGGGGCCTGGCACACAGGCACATGGGAGGGGGCGCGCCGGGAGCGCTGAGCGCCAGTGACACTGCCATCCCCTCCAG
Seq C2 exon
TCCCTGACACAGTTCCTGGGCTGGTCAGTGATGAACACCGACACCTACGACAAGATGAACAAGCTGGAGAACCGCAAGGACATCGCACAGGACATGGTCCTTTACCACGTGAAGTGCGACAGGGACGAGATCCAGCTCATCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000133256:ENST00000255622:9
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.019 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0159021=GAF=FE(27.5=100)
A:
NA
C2:
PF0159021=GAF=PD(5.1=18.8)


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:
GAAGGGGCCCTGGACGAC
R:
CAGGATGAGCTGGATCTCGTC
Band lengths:
294-621
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development