Special

BtaINT0105959 @ bosTau6

Intron Retention

Gene
Description
oxysterol binding protein-like 3 [Source:HGNC Symbol;Acc:HGNC:16370]
Coordinates
chr4:71437181-71440616:+
Coord C1 exon
chr4:71437181-71437311
Coord A exon
chr4:71437312-71440508
Coord C2 exon
chr4:71440509-71440616
Length
3197 bp
Sequences
Splice sites
5' ss Seq
TCCGTAAGT
5' ss Score
10.27
3' ss Seq
CTATTTTTAACGTGTTCCAGGCC
3' ss Score
7.72
Exon sequences
Seq C1 exon
TCTACTTCACTTTAAGGTCAGCTTTTAATACCATATCAACGGAGAGAGAGAAACTGAAGCAACTGATGGAGCAAGATGTTTCTGCCTCCCCCTCTGCCCAGGTCCTTGGTCTGAAGCATGCTCTGTCATCC
Seq A exon
GTAAGTTACACCTCTGTGTCACAGCAAAGCCTGACAGTGTGTCTGGGCTCATGAACTTTTTATGTTTTCCATCGCCATGGTTGTGTTGAAAATTCATGAGAAAACCAAACACATTATCCAAATTATATTCTAACCTTTCATCAGCTTATTCTGCTTATTCTAAACACCAAAGCTGAGCCTACTCCAAATCTTAGTAGCAAATATTTCATTGAGCATTAGATACTCTGTTTGGTTTCCTCCTATTTATCTTGAGTTTTCTGTTTTTGTAAAGCTTTTGTTACGTGTTTGTCTTACTGACATTTGTTTGTTAATGCTTACGAAGTCTGATGGTTTGCAGATTTCCATATCTAAGATTTCACAAGCTTTGACTGATTTTCCAAATTGATAGATACAGGCAGCAGAGTGAAATTTTGAATTCACACTCTTCTCTACAGCCCAGGGTTAATCCTGTTTACCTGTTTACAGCCTATCTCTTTCAAAGACAGGCAAGTGATTTGATTTGATAGTACAAACATTTAGCTCCCACCTGCTCCCCACCGTGGGCACAAAGAGATGAGTCATAAGGAGTGTCAGGCAGTCATTGTGCCTGCTTAATAAACAGAAAAATCACTGCCAAGCCTCAAATGTTTTCCAGTGAGCCAGCCTGTCATTCACGCTCTCTCCTTTTTTCCCCATTGATTGCAGTTTTATTCCTCAGAACTGGGCTGCTTTGAAGTGCAGTGTCCTGGTATTCTATTTTGAATAGCTGACGATATCTGATTGTTCACTCAAAATCTTTCAAAAGCTGGAGAACTTTTCAAAGAACATACTTACTTGCTCCTATGCTTTACTTCTGTGTAGAATCCTTACTATGAAAAGAGAGAGTGTGTGCATACACAATTACCTTCTGAAGTGATACTGAACTTTCTATGTAGGGTCAGGTAGGGGAGATGAATTTTAGGGTCTTGTTTTCAGAAGCTAACTCAAGCAATGAGAGAACTAGAAAATACCCACTTATGCTTTCTACTCATCATGTTACCGAGAGAAGTAAAGTGATGCTTTTGGTATAATGTTAATTGTTAATGCATTAACATTGGTACGTACTGTCATTGTAAGGTACTTAAAGGTGTATTCACTCAGTTGAACATTCCCAGTATGTTATCTTGGAAAGAAATAGAAAATAACATGGATTTACTCCATGTTTAGAGTCTTAATGTTGTCAGCTAAGAGGTAGAAACACCCCCTTTTGGATTGTACTGGACAGTCAGTCACACACAATCTGCTACTTTGGTTTGAGAGAAGCAGTGTGGTTCTTTACTTTTTTTTTAAGTTTATTTTTTAGTGGTAAAAAGCACTTCTTTATTCATTTGTGTCATTTCTTTGTGGCCCAGCCACCCAATGGAATATTATTCATCAATAAAAAGAAATGAGCTCTCAAGCCATGCAAGATATGAGTGAATCATAAATGGATATTGCTCACTGGAATAAGCCAGCCTGAAAAGACTATGTACTGATCCATTCATATGATATTCTGGAAAAGCAAACATACAGAGATAATAAACAGATTACTGGTTGCCAGGGTAGGAGGGAAAGCATTTCTTATTGTTCCAAGTAGGTTGGCTTTTAGTGCATTTAGAAGGTACCTCTGATGGGCTTCCCAACGGCCCTTTCACTGTGGTCTTCCTCTTCCCTGCCCTCCTCCTGTGTGAGGTCCAGCTTCATCTTGTTAATCTGCTGGTCTGGTAGAGGCCGTGAGACCCAGTTGGCCCTGGCGTCCCTGGCCACAGTCATTAGAAAGTTGAGATAAAACAGAATGATCATTAACTTCTTTTTTTGTCTTGGATTCCTGATTAGATTCAAGGCTTGTTTTTTAAAAATAAAAATTTGAGAGTTATCTCAGGACTATCAGAATGAATCTGTGTTGAATGTACAACCTTTGTGTGTGATTTTTTTTTTTTTTTTCCTGCCTGTGGCTCACAAAGGAAAGAAAAGCTACTAAAATAGCATATATTTCAGGCTATCTGGAGATTCTAGCCACTGGTATCTATCTATTCTAGCCACTGTGTAAGATGCCAGCAACATATTGGCCAAAGTGAGTGCCCCATAGAGGTTTTTAAATGTAGTTGTGTGCTTTAAGACACATTTACTTAGTGTTTCCTAAATGACCCTTCAGAATTTCCAAATAATCCATTCCAACTGTGGATACTAAAAAATAAAGCCAAAATTCTTGTTTGAGATCCAGGCAGTGGGTGAGATATGAACACTCTTCTGTGCTCTCAGCAGGTATACCCTATGGACCCTGATGGATGGGAAAAGGCTCTGAGCTTCTCAGAAGAAAGTCAGGAAGGCAGGTGGACAGGATGGACAGATGTACAGGCGCCTGGGAAACTGATTGTGGGAGTGGGTAGGAGACAGTCAGGTGAAGTTGTCCCTTTCAAAGACAGATCATTTGAAGGATGCTGGTCATGAAGCACAGGGGAGACCAGCATGAAGGAAAACACCTTCCTTTACCTTCCTAGTTGGGAGGATGGGCGGGGGACTCAGACCTGCTCAGGGAGAAGAAGTAAAAGAGGTCCAGGTGGGCTGACAAGAGCTCACAACCCCTTCCCAGGGCCCTGGTGCTTAGCCCCCATCCAGGTAAGTGAGCTCTCTCTCTTTTATTTTTTTTTTAAATAGACTATCTTAGTCATGAAGAATGAACATAAAACAATCAATACCTATGTTATAAAACAGTAAAATTAATCCTCTGCAAAATCTTACTTCTCAGCACACTTTCTAAGACCCCACTCAACCAGTGTGACGGAACATTAAAATATGGCCAGTCACATGGAGGTGAGAGCGGCGTTTTTATTACAGATGAGAAAGGAGCTTGGAATCTTTAGGGGGAGCTGTTCAAAGAGACTGAAGGCAGCTGAGGAGGAGGAGGGGCCAAGAAACCAAGAGCAATAAGGGCTTATAGGTGTGTGTGATTTCCTTCTCCACTGAAAGAAAAGCCTTACTAACCCTTACTTTCATCCCTGGAAATGAGAGTCGAGAAGGGTCTGCATTCCCAGTGTTTAATAGCTTGTATCTGCCAGGCACCAGTATCCTGTTGGATAACATTCAAGAAAGAAGTCCAGGAGGTGCCCCCGTGAGGGCTCCTCCACACTGGGCTTACTGCTGTGCTTTTGGAAACATCCATTGATTAACAGAGCCCCACTATTTTTAACGTGTTCCAG
Seq C2 exon
GCCCTAGCACAAAACACAGATCTTAAAGAACGCTTATGCAGAATCCATGCCGAGTCTCTGCTCCTCGACCTCCCTGCTGCTGCCAAGTCGGGTGACGGTCTGGCAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000019342:ENSBTAT00000025767:10
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.205 A=NA C2=0.167
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
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]