Special

HsaINT0118693 @ hg38

Intron Retention

Gene
ENSG00000079156 | OSBPL6
Description
oxysterol binding protein like 6 [Source:HGNC Symbol;Acc:HGNC:16388]
Coordinates
chr2:178331552-178332754:+
Coord C1 exon
chr2:178331552-178331605
Coord A exon
chr2:178331606-178332640
Coord C2 exon
chr2:178332641-178332754
Length
1035 bp
Sequences
Splice sites
5' ss Seq
GATGTAAGT
5' ss Score
9.11
3' ss Seq
TACTAGTCTTTTGATTTCAGATT
3' ss Score
5.51
Exon sequences
Seq C1 exon
CGTTTTTTTGTCCTGGATAATGGAATGTTAAAGTATTCAAAGGCACCACTCGAT
Seq A exon
GTAAGTAGCACACAGGACATGTTTCAAAGGTTGATTTCGAATTCTGCTTGAAGTGAGTAAACACTGTAATTGTACAAGCCTTGTGCCATAGTTACCAGCTTTGTGCATGTCTGGGCCTGTAAGATTTCACAAGCTCCCAAACCTCCATGTTCTAAAGTGTGTCAACCTAGTGCATGAAGATTTAACTATTTTGATGTGTGTTATTAAAAACAGAAGCTTAAACCTTAAAAGTGACGCATGAGTAAAATCACCTTCTGTCACTTGGATAGAAAACGCAAATGGGCTTTTTTCCTCCATCTTCCAATAAACTCTGCTTTATGTGTGCTGCTCTGTTCTTGTCAATGTCCTTTTAAAAACTATCTTACAAATTTTATTTCTACGTCATACATCTTTTTATCTTGGAGATCCCAATTCACAAAAATTATTTCAAATTGTTTTTGTTTAGTATACAAAGGAGTAGTTTGCATGTAACACTGGAAAATTCCTTCCTTCATCATTGTGGTGTAGGGGAAGTAACTGAAGGCTTAGGTTTCAGTTTTGTCCCCATCCCTGCCATTGAATCAGCCATGTCCTTGATCAGTGGAGCAGCCAGAAGGAAGAGCTGGCTGCTCCTTGCTTTCTGGTCCCAGCTGCCCTGTTCTGCCCCAGCAGCTGTCTGCCAGCTGATTACTCAGGGATGTTCTGGGTTATACGTCAAAGATTGACCGCAGTTATTTTAGGACCGCTAAAGATGTCCTTTTGGGAGAATATAAGCTGTGCAATCTAGAATTATGAAGAATTAGTATTACATTCTATGCCAAAACAGGAATAAGATGAATAGTCTTATTTATAAAAATTGACGTGAAGTCACTGCAACATCAACTGTCCTAGAACCTAATCCATAGAACCTTAACTATTTTCTGTTTGTTAAGGAGGTATATGTAGTATTCCACTTCCCATAGATAAGTTAAAGATTACTTTGAGTTCACTTAAATACAGTACAGAAACATCAAATCATATATCCTTTCAGCCTATTTACTAGTCTTTTGATTTCAG
Seq C2 exon
ATTCAGAAAGGAAAGGTCCATGGGAGCATAGATGTGGGACTCTCAGTCATGTCAATTAAAAAGAAAGCTCGAAGAATAGACCTTGACACCGAAGAGCACATCTATCATTTGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000079156:ENST00000190611:6
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:
PF154091=PH_8=FE(18.9=100)
A:
NA
C2:
PF154091=PH_8=FE(41.1=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
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