Special

HsaINT0152524 @ hg38

Intron Retention

Gene
ENSG00000198569 | SLC34A3
Description
solute carrier family 34 member 3 [Source:HGNC Symbol;Acc:HGNC:20305]
Coordinates
chr9:137234416-137234731:+
Coord C1 exon
chr9:137234416-137234532
Coord A exon
chr9:137234533-137234606
Coord C2 exon
chr9:137234607-137234731
Length
74 bp
Sequences
Splice sites
5' ss Seq
TGGGTGAGC
5' ss Score
7.23
3' ss Seq
GTGACTCCCAGTTCCCCCAGGGG
3' ss Score
3.56
Exon sequences
Seq C1 exon
ACTTCCCCTTCCCGCTGGGCTGGCTCGGCGGCTACCTGGCCGTCCTCGCGGGCGCCGGCCTGACCTTCGCACTGCAGAGCAGCAGCGTCTTCACGGCGGCCGTCGTGCCCCTCATGG
Seq A exon
GTGAGCAGGCAGGACAGAGGCCTCGGGAACGGGGGCTCGGGCTGGGGTCCTGTGGTGACTCCCAGTTCCCCCAG
Seq C2 exon
GGGTCGGGGTGATCAGTCTGGACCGGGCGTACCCCCTCTTACTGGGCTCCAACATCGGCACCACTACCACAGCCCTGCTGGCTGCCCTGGCCAGCCCCGCAGACAGGATGCTCAGCGCCCTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000198569:ENST00000361134:11
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=0.000
Domain overlap (PFAM):

C1:
PF0269010=Na_Pi_cotrans=FE(27.9=100)
A:
NA
C2:
PF0269010=Na_Pi_cotrans=FE(29.3=100)


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:
CTGACCTTCGCACTGCAGAG
R:
GCTGAGCATCCTGTCTGCG
Band lengths:
174-248
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains