Special

HsaINT1025832 @ hg38

Intron Retention

Gene
Description
otogelin like [Source:HGNC Symbol;Acc:HGNC:26901]
Coordinates
chr12:80261969-80265210:+
Coord C1 exon
chr12:80261969-80262093
Coord A exon
chr12:80262094-80265000
Coord C2 exon
chr12:80265001-80265210
Length
2907 bp
Sequences
Splice sites
5' ss Seq
ACAGTAAGT
5' ss Score
9.49
3' ss Seq
CTAATTGGGCTCTTTGTTAGTTG
3' ss Score
2.41
Exon sequences
Seq C1 exon
TTCTCCATCAGGCATGATAGAAGGTACACCACAACTTCACGCAAATGCGTGGAGAGTTTCTTCTACCTGTTTTGCACCTGTTCATGTCCCAGTGGTGGACCCCTGTAACATCAATCAACAAAACA
Seq A exon
GTAAGTTTTGCATGTAAACTTCCTTTCTGCTGTAAACTTAGGGAAAAGTTCTATGTATTACTATAATTTTATAAAATTAGATAGTTTAAATTCTAATTTTCTCCATTATGGTAAAATCAATGCCATTCCTCGTGTATTTTTTTTTTGCTTAATATTATGCCTTTACATATGTCTTTTCATGTAATCTAGGTTGTTTTTTAAAAACCTGACAGTGGCTTTTATTTCCTATTTTTATTTCATAAATTTTCTTATTTTAGATGTTTAGAAATCCCTTGTTTGCAGATGTGGACTAGCATTTGGGAGTTTTCAGAGTCTTTAAATACTAAAGAAAAGCCTCTAGGAATCCTCTGAGAATGCTGTGATAGTCCAGGGATGTTCGATGTCAGTTATTACCATCTCATTACTCATTGCTCATGAGCCCTACTCATAGCATATATTATGGCTTTATAAGCAGGAAGCCAGTGATCCAAAGAGGCTTTGTGCCATTGAGTGGGCAACAATTTGAGATGGTCATGCTCCAGAGTTCCAATTTGCAATGACAGGACAACTCACATGCTAAGAATTTTTGGCTGCATTTTTTAAAACTAAAGCCCCAGCAAACCATGTTAAAGTCCAGTTCACTTTGCAATAAAAAAGATATACATGTATATATTCAGATAGAAGATACACATGTATATATTCAGATAGAAGATATATACAAGACATACACATGTATATATATAATTGTGAAAAAATTAATGTACATGCTTAAATATTCTTATAAGTTTATTTTTTCCTTTAATCATCTTGGCTAGTTCACTATTTGGATGTAGTTTTTAAAAATACATTACTCATATTGGTTGAGCTTTCATAAGAAGCCAGCACAGTTTACGGATCATGCGGTGGTTGTTGGGAGGATTCTGTTGATTGCCATATTGTTTTTATTATTAACATAGGATTCTGGTATGCTGGAAAGAGCAGAAGATACTTTTGCTCTTTGTGCTTTCTGTCTTTTTTAAATCTAAGCCAGCTTTTAAACTTGAAAACGTTTCTTAACCTCTTTGATCATTTTTCTTATCTATAATAACACGGCTAGACTAGAGTTTTTTAGTTTCATGAATGACTACTTTTAATCTCACTCCCATTTAACAATACCTTCCTCCATTCTGTCCCCAACTTTCAACTAATCTACTCCTCCTCCTTCAACTACTCTTGTTTGGTTTGTTTCTTTCTTGGTTTCCTCCTGGATATTGTAGCAACTTTACTTTTTATTTTTTAATAACATGTTAAAGTTGAAGTAGAGTTCAATTGATAAATTCAGTTTCCCTGTGGTCATTTCTTTAGTTACCTCCTTTATTATATGCTATTTTGCTCTATTTTCTATCACTTTTCTTCCCATATCCCATGTCTTTTAAATATATACATACACGAAATTGAAATATTAAACTGGATATATAAACTATTTATATTTTGAGATATTTGCCTTGTCTTTGAAAATAAGCCTGTGAACTACCCACATTAATTTCCCCACATGGACCCTAAACCACACACATGCTATGTACATGCATACATATATTTGATATTAACTTTTTTTTAGCTTTGCCATGAACTGTGATTTTTTTTTAAAAAAATTCAAATAGGTAAATTCAGGAAGATCCTCAAAGAAAGGAAAATAAGTAGACAAAAGTCAATAACTCTGATCTAGATTCTAAAGGATTTTTTTTCATGAGGATCTTCTTTAGTTATCCTTAACTTAATGTCAGTGGGAATATACTTTGATCTACAAATTGTTAGCCTCTTTGGTGTATTACTTTGCTCTTTCAGGATCCTTGGCATTAAGAATATATATGTAAACAGTATACTGCTATAGTTTAAGTCATTTGTTTTTATATACATATACATTCTGAATGCAAAAATATCATACTTGAGCAATTATCATGTTTTCTTACCAATAATAAATATATGTAATATACTCAACAAAATAAGTTCAGTATAATTCCTTAGTAGTGAAAAAACTGATCTCCAACAGCTTATCTGGTCTGTAAAAGACAATGACAATGAAAAGATTGATTAATTTTATCTGTTAGGAAACCAAGGAAAACTAGGTCCACGATATCAAGAAACCACAAACCTACCCTCTTTCAGAAAGATGGAATCTGAATTGTTTTGTCAAACTTGGTTACTTCTATAAAGAATTATATCTGATCAGTCATTCTCAAGGGAAAAATCAACAGATTTCAGGAAATGATTACACAGATGTCCTCCCCTCCCCAGGTGATTTTATAGTTACATCTCATGGCCTTCAGCATATACCCTAATCCCCAATTTCTACTCATTATTCACTTATTCATGCATTTATAGATTTATTTATCAAACATTATTGAGCTCCTAATATCTGCCAGACATTGTACACTGTGCATTGTGCAGACATTGAGTTCAACAACTATGTGGCATCTGACACATTACCATTCATTTCAGAGACTCCATTGAAATGAGATCATTCCCAATTCTTCCTAGACAATTGTGTATTACACAGGGTTGCCATAATATCCACAATCTGGAACCACTTTGTTATATGTGGATGTCTGGAAATAAGCCTCCCAATACTCTCCAATTCTTTATAGTAGGTTTCCTAAGATGATCCTCATGCAATGGGATGGTTGAGGCCACTGCTTCTCTCAACCCTTCTATTACTCATGTTATTCAGGTACAATACACTATTTTTTTTCCTAAAAGTCTGTTGAATGTGGATTAAGTGCTGTTACCAATATTATATAAAAAAAACAAAAACTGTATAAGCTGAAATTGTTCACTCTTGTATTAAAAGTAATATGCACTACAGTGTATTTCTAAGAACGTGAAATGCTTGGATAATTCTGGGGTAAGATCTGAACTGTTAAATAAGATGCTAATTGGGCTCTTTGTTAG
Seq C2 exon
TTGGGTATGCAGCACACTGTGATGTCATCCACCAGGAGCTCTTTGCTCCTTGCCACATCTATATTAGCCCTGGGCTGTACTATCAGCTATGCCGCCACGATGCATGCAAGTGTGGAAGCTCCTGCCTGTGCAATGCTCTTGCCCACTATGCCTACCTCTGCGGCCAGCACGGTGTTCCCATTGATTTCAGAACTCAGATTTCTTTCTGTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000165899:ENST00000547103:18
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:
PF0009420=VWD=PD(3.3=11.6),PF087426=C8=PU(0.1=0.0)
A:
NA
C2:
PF087426=C8=WD(100=100.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
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]


SPECIAL DATASETS

  • Autistic and control brains