Special

HsaINT0025313 @ hg38

Intron Retention

Gene
ENSG00000198917 | SPOUT1
Description
SPOUT domain containing methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26933]
Coordinates
chr9:128826022-128826433:-
Coord C1 exon
chr9:128826384-128826433
Coord A exon
chr9:128826153-128826383
Coord C2 exon
chr9:128826022-128826152
Length
231 bp
Sequences
Splice sites
5' ss Seq
CAGGTAACG
5' ss Score
10.52
3' ss Seq
TCCCGGCTCTGCCTCCACAGGGC
3' ss Score
10.84
Exon sequences
Seq C1 exon
GTACCTGAGGAAGGCGTTCTTCCCCAAGCACCAGGATCTACAGTTTGCAG
Seq A exon
GTAACGCTGTATGGGCCCGCCCCCCCATTTCCCCTGGATCATGCCACAGACACTGAGACCACCCAGTCCTACCCTGCGCTGTCCAGGTGGGAAAGCAGGCCTGGGAGAGCAAGACCTGTGTCTGATGCCAAGACGCAGGTCTGTGGCAGAGCCGGTACTCCGCTCCAGGGTCCCCACTGCACCCTGTGTGCCCTAGCACTTCCCAGACTCTTCCCGGCTCTGCCTCCACAG
Seq C2 exon
GGCTCCTGAACCCCCTGGACAGCCCCCACCACATGCGTCAGGATGAGGAATCCGAGTTCCGAGAGGGCATCGTGGTGGATCGGCCCACCCGGCCAGGCCACGGCTCCTTTGTCAACTGTGGCATGAAAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000198917:ENST00000361256:6
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=0.432
Domain overlap (PFAM):

C1:
PF0259812=Methyltrn_RNA_3=FE(5.8=100)
A:
NA
C2:
PF0259812=Methyltrn_RNA_3=FE(14.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GAAGGCGTTCTTCCCCAAGC
R:
CTTTTTCATGCCACAGTTGACA
Band lengths:
172-403
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