Special

HsaINT0020291 @ hg38

Intron Retention

Gene
Description
otogelin like [Source:HGNC Symbol;Acc:HGNC:26901]
Coordinates
chr12:80328665-80329109:+
Coord C1 exon
chr12:80328665-80328744
Coord A exon
chr12:80328745-80329050
Coord C2 exon
chr12:80329051-80329109
Length
306 bp
Sequences
Splice sites
5' ss Seq
ACTGTAAGT
5' ss Score
8.59
3' ss Seq
GCACCTTTGTTTCTTTGTAGGTA
3' ss Score
10.49
Exon sequences
Seq C1 exon
GGTTGAAGGATGCTTGCCCTACTGCCCTAAAAATATGATCCTTGATGAGGTCACCCTCAAGTGTGTTTATCCACGAGACT
Seq A exon
GTAAGTGTGAACGTTGCTTAATTTACTCTGAAAAATTATACGCTTGCATATGTTTTTTCCGAGGCAAGTGGTTGTAAACAGAAGTTTTAAACAGACAATCAACTCTCATAAGATTATTCTTCAATGTCTCTTACATAGCTTTTTTTCCCTAATTACTTTTTAAATCATGTAGATCTTCCACTAACATCTCTCCTGCATTCTTTTTCCCAAAACATTTTCCTTGAAGCTAAAGAGTCCTCTATGAAATATGTGGGTCTAATTTTATGCAAATACAGTTTTATAAAGAGCACCTTTGTTTCTTTGTAG
Seq C2 exon
GTATACCTGTGATTCCCACAGAACCAACATTAATGCCACCAGCTAAGCCAACTGTGCCC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000165899:ENST00000547103:35
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:
PF0182612=TIL=FE(48.2=100)
A:
NA
C2:
PF0182612=TIL=PD(0.1=0.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
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