Special

HsaINT0025311 @ hg38

Intron Retention

Gene
ENSG00000198917 | SPOUT1
Description
SPOUT domain containing methyltransferase 1 [Source:HGNC Symbol;Acc:HGNC:26933]
Coordinates
chr9:128826540-128827191:-
Coord C1 exon
chr9:128827032-128827191
Coord A exon
chr9:128826630-128827031
Coord C2 exon
chr9:128826540-128826629
Length
402 bp
Sequences
Splice sites
5' ss Seq
CAAGTAAGG
5' ss Score
7.66
3' ss Seq
CCCCATCTCTCTCTCTCCAGGAC
3' ss Score
13.24
Exon sequences
Seq C1 exon
GGCGGCCCTACACACTGAGCGTAGCCCTGCCGGGCTCCATCCTGGACAATGCTCAGTCGCCGGAGCTTCGCACCTACTTGGCCGGTCAGATTGCCAGAGCCTGTGCCATCTTCTGTGTGGATGAGATCGTGGTGTTTGATGAGGAGGGCCAGGATGCCAA
Seq A exon
GTAAGGGGCCATCCCACAGGGTGCCAGGGTTCAGGGAGAGGGAGGGGCTGCCGGGATGGGCCGAGGCTTCACCATGGCCCCGTCCACATGCCTGGCTCTTCCCTCGTGCCCTGCCTGAAATATTCCCTGTGTAATCCTTAGTGGGTAGAGTTGCCAGGTGGGGGTGATGACTACAGAGGTGGGATTGGGAGCCAGAAGGCCTAAACCTGTATCTCAGCTGTCACCCCGGCTGGAGTGCATGCAGTGGCATGGTCATGGCTCACTGCAGCCTCTACTTGCTGCACTCAGATGATCCTCCCACCTTAGCCTCCTGAGTAGCTGGGATTATACGCGTGCACTTGTAGACAGGAGCTCTTGAAGGGGCCACAGCTGGATCCTGAGCCCCCATCTCTCTCTCTCCAG
Seq C2 exon
GACTGTGGAGGGGGAATTCACAGGAGTTGGGAAGAAGGGGCAGGCGTGCGTACAGCTGGCCCGGATCCTGCAGTACCTGGAGTGTCCACA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000198917:ENST00000361256:4
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=0.097
Domain overlap (PFAM):

C1:
PF0259812=Methyltrn_RNA_3=PU(16.8=90.7)
A:
NA
C2:
PF0259812=Methyltrn_RNA_3=FE(10.3=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGCGGCCCTACACACTGAG
R:
AGGTACTGCAGGATCCGGG
Band lengths:
238-640
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