Special

HsaINT0161437 @ hg38

Intron Retention

Gene
ENSG00000116266 | STXBP3
Description
syntaxin binding protein 3 [Source:HGNC Symbol;Acc:HGNC:11446]
Coordinates
chr1:108779286-108782517:+
Coord C1 exon
chr1:108779286-108779410
Coord A exon
chr1:108779411-108782421
Coord C2 exon
chr1:108782422-108782517
Length
3011 bp
Sequences
Splice sites
5' ss Seq
CAAGCAAGT
5' ss Score
2.32
3' ss Seq
GTGCTTCTGTCTACTTGTAGATA
3' ss Score
10.24
Exon sequences
Seq C1 exon
GGTAAAACTCATTCACAGCTCTTAATAATTGATCGTGGCTTTGATCCTGTGTCCACTGTCCTGCATGAACTGACCTTTCAGGCAATGGCATATGATCTACTACCAATTGAGAATGATACATACAA
Seq A exon
GCAAGTATAACTTGAAGGGCATATAAAGGGCATATACAAACAGGATAGAATATGAGCATTTAATGATTTATATAGGCACCAGAAATCTGAAAGCCCCTATAACCTTTTCTATTCAGAGACTTTATCCTTCTCTTATTCCTACAGTTATAGTCTTTGACAGATAATGTTGACCTTGTAAATTAAAGTGTAATTTGATTGCTTTGGAGCATTTTTGGTGTGTTTGCTTCCTTAACTGTGTGTACAGTAGAGCTACATTTAAACACAGGGAATTTGGCCCTTTTGCTTTTAAAAGTAAATACCAGGCTCACTATCATTGAAGGAGAAACCATATTCAAAATTGTTAGGCTATAATTGTTCTGAATCATACATTCAAAAGTGTATGTGTCTTATCAACATAAAGTATTTTAAAAGATTGGAACACTAGAAAACTAAATAGGATGGCTATTGAGGACAACAGGCATAGTTTTACCATTTTGGTACCTTCTACTGAGTTAATCTTGGTATAAACATATTTACTTTAAAAGTAATGTCAAATAAAAACCTAAATGAAAAATGAAATAGTTTTCTATCAAGGAATCATCTTACTGTATCTCTGTATCATTTATGGTGTATGTGTTACATACATTACAAATGTTATTTGATGTCATGATTTCTGAATCCAAACTGGTATTTGTCAGCTAAGATTTACTGCTTGAGTACAGTAATAAAAATGAAAATAGTTTTCTGAAATTTTATGTTTAAACTAATTTGTTAGTTTTAAGATACAGACACTTGTGATAGTTATGATACTGTTTTTTTTCTTAAATATTGTTAAAATTTGTATTTTCTATTGTATTTTTATTTGCATTCTGGTCAAATCTTGGTTTCTGAGTTTTTCTCTGTATTATCTGTATTAATGTTAGATAACATAGCTATTTTTCTAATATAAAAGTTATTTTAAGCAGTTTATTCAGAGGGGATATTATTTACCTCTGTTACCCTGTAGGTCTCTAAACTTTTAAGTAGACTTATTTTTTAAAAAGCTACTATACTCCCTTCTTTCTGAATCAAAAACATTCAGAGATAAGAATTAGATGGAAGTAAAGCTCCCTGTGGTTTGTGCTCCATCACAATTTTTTTTTTTTTTTTTTTTTTTTTTAGTAGAGGCAGGGTTTCCCCATGTTGGCCAGGCTAGTCTTGAACTCCTGACCTCAGGTGATCCCCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGGGTGAGCCACCACGCCCAGCCTTCATCACAGTTTTTTATGGAAACAGAATACAAAGCAGCAGGAAGCTCTAAGTGTCCAGATTCAAGTTTTCATGTTGGTGCCTTCTTTAAATTTACTTTTTTTTTTTTTTCTTTTTTTGAGACAGAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCGATCTCTGCTCATTGCAGCCTTCGTCCCCTGAGTTCAAATGATTCCCAGCCTCAGCCTCCCAAGTAACTGGGACTACAAGTGTGCACCACTGCGCCTGGCTCATTTTTGTGTTTTTAGTAGAAATGGGGTTTTGCTGTGTTGGCCAGGCTGGTCTCGAACTCCTGGCCTCACATGATCCACCCACCTCGGCCTCCCAACTAAATTTACTTTTAAAATGGGATATTCATCACCTGAGTATTGTCAGGCTTGTTACTCTTATCTCTGTTTACAGATCACTTATAAGTCAAAGGTATTGTGTAAGAACAAAGTGGTATTTTAAATGACAAAAGGGCTTTCATCCTTAGTGCAGCCTTATATAATTGAGCACAGTGATTCTGTCTTTGGTCATCTGTAATCCACACAGGTGGATGGTTTTATAGATTGATGTGTAATTTGTGGGGGTTATAGAAACGATTATATTCATATAGCAAAGTCTATATGTATTATTTGTAGTTCAGAGCTAGGAAAACTCAATGCAGTCCTTCCTGATCTTGACTCAGGAAATCAGTAGTTCCAAGGATGATTCAGTCTTGTCTAGTTCCACAAATGGAAGGAGGGTGTCTGCATAAAAAGATAAGGGGAATCAGTCAGGAAGCCCATTTTGAATAGCTTCATGAATCCCTTAAATTGTTGCTCACTTCAGCAGAACTCATTAAAGCTATCACAATTTTTATGGCTTACATTAATTTTTTTTAATCTCATTTTCTTTCTCATTCTGTAAAGGAGATGTGGTTATAGGGTTGGGGGAGAATAAAGAAACAGATGATAAATGTTTGTGAATTTTGTACCAATTCTGAAACACCTTCAATATTTAATAGGTTATATTGGGGAGGATATTCCTGTTTTGTTTTGTTTGAGTCAGAGTCTTGTGCTGTCACTCAGGCTGGAGTGCAGTGGTGCGATCTCTGCTCACTGCAAACTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCAGAGTAACTGGGATTACAGGTGTGTGTCACCACACCCTGCTAAGTTTTTGTATTTTTTTTTAGAGACAGGGTTTCACCTTGTTAGCCAGGCTGGTTTTGAACTCCTGACCTCAAGTGATCCGCCCACCTTGGCCTCCGAAAGTGCTAAAATTACAGGCGTGAGCCACTGCACCTGGCCGATATTCCTGTTCTTAATGGAAATTTGATAATTGTACTGTGGGTTATTAGCACATCAAAACAATGTTGTAGGGAATTAGAACACAAAGCGTTAGTATATTGAGTCTTGTTCTTAAAGTTAACTGTAGGACGTTGAATTTTTTTTATAAAGTACAATTTTGCTGAACTAAAACTCTAATAATGGCACCTAAACTGAATATTTGAAAATGTCTTGGTAGGCTTAGGACTTATTTTTAATGTAAGGATAGCAGCGTGCCTTAGTTTTGAGTAGGTATTCATTACCCCCCTAAAATAGTGGATTTTACTTTTCAGTTTCTTGAGTTGTGTCTTGAAATTATTGTTTGTAAAAATGTTTCTTTTGATTTTGGAGGGAAAAAAATCAAAAAGTTTTAGTGCTTCTGTCTACTTGTAG
Seq C2 exon
ATATAAAACAGATGGAAAAGAAAAGGAGGCCATCCTTGAAGAAGAAGATGACCTCTGGGTTAGAATTCGACATCGACATATTGCGGTTGTGTTAGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000116266:ENST00000370008:9
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=0.015
Domain overlap (PFAM):

C1:
PF0099518=Sec1=FE(13.9=100)
A:
NA
C2:
PF0099518=Sec1=FE(10.9=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping 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

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains