Special

HsaINT1025851 @ hg38

Intron Retention

Gene
Description
otogelin like [Source:HGNC Symbol;Acc:HGNC:26901]
Coordinates
chr12:80238851-80239439:+
Coord C1 exon
chr12:80238851-80238978
Coord A exon
chr12:80238979-80239332
Coord C2 exon
chr12:80239333-80239439
Length
354 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAAT
5' ss Score
8.39
3' ss Seq
TGCCATCTTTTTTTGCACAGGCA
3' ss Score
8.6
Exon sequences
Seq C1 exon
AGGACTATACAGAAGACATCGCTATGTTTGCAAATAGTTGGTCGGTGCAAACTCCAGATGACACCAAATGTGTACTCACACCCTCAGATTTTCCAAATCCGTGCTCCAGTGGAATGCCAGCATTTGAG
Seq A exon
GTAAATTTGATGTGAGAAATGTGGGCATGTCAGACAGAATACACATATATCTTATTTGTATAATTAACTAAGCATTTTTTAGTGTAAACACAACATAATTTAAAAATATTATATCCAGGAAATGTAATTGCAATAGGAAATCACCTTAATTTTAGAAATAGTGAATGTAGTGAATTTCATAAATGCAGTACTCATGAAAATAATGTAGTCAGAAAAATGTTAGTTAAAATGTATAAGTTACCATCTTTTTCCTTGTGAGAACTGAAAATCTTGCAAATAGATCTGTAAAAATAATAGAAGACTATACACATACCATGAAACATAGTCTAGTGACTGCCATCTTTTTTTGCACAG
Seq C2 exon
GCAATCTTCTTCAAGTGTCAGATACTGTTGCAGTTTCCTTTTCTGAGCTGCCATGAGTATATCGATCCATACTTATATATTGCCAGCTGTGTTAATGATCTTTGCAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000165899:ENST00000547103:9
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:
NO
A:
NA
C2:
PF087426=C8=PU(45.2=91.7)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
AGGACTATACAGAAGACATCGCT
R:
GCAAAGATCATTAACACAGCTGGC
Band lengths:
233-587
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains