Special

MmuINT0071216 @ mm9

Intron Retention

Gene
Description
otogelin-like [Source:MGI Symbol;Acc:MGI:3647600]
Coordinates
chr10:107235378-107235857:-
Coord C1 exon
chr10:107235778-107235857
Coord A exon
chr10:107235417-107235777
Coord C2 exon
chr10:107235378-107235416
Length
361 bp
Sequences
Splice sites
5' ss Seq
ACTGTAAGT
5' ss Score
8.59
3' ss Seq
GCATCTCTATTTATTTGTAGGCA
3' ss Score
6.87
Exon sequences
Seq C1 exon
GGTTGAAGGATGCTTGCCATATTGCCCCAAGAATATGATCCTGGATGAGACGACTCTTAAATGTGTTCACCCAGAAGACT
Seq A exon
GTAAGTATGGACCTTGCTTAATTTACTGTTAAAAATAAAAAGCATAGATAATTTTTCCCTCAGGCAAATGGTTACAATTAGAAGCCTGAGACAGAGAATAAGAACTCATTTCAATCTCCAGTCCATGGAGCTAAAACAAACAAACAAAAAAACCCAACAACAAAAAAATCAACCAACCAACCAACCAGACAAAATAACTTCCCAATTATTTTCTAAAACATTTATGTCTTGCTTCTCATATCCCTCTTTTATGTTTTCTTTCTTAAAATATTTTCCTAGAAGACAAAGAGCTGTATGTAAATTAGGTGGGTCTTCTTTTATGGAAATATAGATCAATGCAGGCATCTCTATTTATTTGTAG
Seq C2 exon
GCATACCACTGTTTCCAACAGAACCAGCATTGCCACCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000091455-Gm6924:NM_001177567:35
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.143
Domain overlap (PFAM):

C1:
PF0182612=TIL=FE(49.1=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:
NA
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

  • Pre-implantation embryo development
  • Muscular differentiation time course
  • Spermatogenesis cell types
  • Reprogramming of fibroblasts to iPSCs
  • Hematopoietic precursors and cell types