Special

HsaINT0118719 @ hg19

Intron Retention

Gene
ENSG00000006025 | OSBPL7
Description
oxysterol binding protein-like 7 [Source:HGNC Symbol;Acc:16387]
Coordinates
chr17:45894146-45894725:-
Coord C1 exon
chr17:45894622-45894725
Coord A exon
chr17:45894239-45894621
Coord C2 exon
chr17:45894146-45894238
Length
383 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGA
5' ss Score
10.77
3' ss Seq
CCCCCACCTTGACTTGCCAGGCC
3' ss Score
6.97
Exon sequences
Seq C1 exon
AGCTCTCTGAGTGTCAGGGGAAGCTCCAGGAACTACACAGGCTCCTCCAGAGCCTGGAGTCCCTGCACCGAATCCCCTCAGCCCCTGTTATCCCCACACACCAG
Seq A exon
GTAAGATCCAGGGGTACACACAGGGTCCTGCTCAGGCCCCCGATCCCATCACTTCCCCAGGATGGGTCCTATTCCTCCTACATCGCTGCAGTTTCCTGGAGAGCCATGCATCGCCTGGTTTCCTCCCCACCCCTTACCCATGTCCAAACTGTATCAAGATTGTCTCTGTTCCTCCATGCCCATGCCTCTGCCAGGGTGGCTGTCATCTTCCACTGGGATGTCAGTTGTCTCTGTCGCCCTGCCTGAGCGGCCGCATCCTCTGTGCTGGGTAATCTGCGCCCTCCTCCATGGCGCAGGAGGCCGTCTACCTCTCCCAGGCTGTGATGGTTTCTGCCCCTTTTCCCCACCCTGTGAGTAAAATTGCCCCCACCTTGACTTGCCAG
Seq C2 exon
GCCTCAGTGACAACCGAAAGACCCAAGAAGGGGAAACGGACAAGCCGCATGTGGTGCACCCAGAGCTTTGCCAAGGATGACACCATTGGACGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000006025-OSBPL7:NM_145798:8
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.229 A=NA C2=0.645
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Chicken
(galGal3)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TCTCTGAGTGTCAGGGGAAGC
R:
CCAATGGTGTCATCCTTGGCA
Band lengths:
190-573
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development