Special

HsaINT0082800 @ hg38

Intron Retention

Gene
Description
integrin subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:6153]
Coordinates
chr10:32922257-32922735:-
Coord C1 exon
chr10:32922640-32922735
Coord A exon
chr10:32922347-32922639
Coord C2 exon
chr10:32922257-32922346
Length
293 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAAT
5' ss Score
8.88
3' ss Seq
GTTTTATCTTTTAATTGCAGGAG
3' ss Score
8.74
Exon sequences
Seq C1 exon
GATTATCCTTCTATTGCTCACCTTGTCCAGAAACTGAGTGAAAATAATATTCAGACAATTTTTGCAGTTACTGAAGAATTTCAGCCTGTTTACAAG
Seq A exon
GTAAATGTGTGAGATAAAAAGAACAAGATTCTAAACATTTTTGATTGTTAGAGGCAAATCATGTCTGAATTGAAATGTGGGAAAATGCCACCAGATAGGCAAACCGAATTTTACAAAAGTGGTTTATATTAATTTTTAATCACATATTATAAAACTGGTTTCTAGGTTTGACTCCTAAAGTTAGTTAGGAGGAAACATGGGAACTGGCATTTAAAGATAAAAGTTGCTCAGTGGATCCTAATTGGTTGAATGAATAGCAGTTGTATTTTACGTGTTTTATCTTTTAATTGCAG
Seq C2 exon
GAGCTGAAAAACTTGATCCCTAAGTCAGCAGTAGGAACATTATCTGCAAATTCTAGCAATGTAATTCAGTTGATCATTGATGCATACAAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000150093:ENST00000302278:8
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:
PF0036213=Integrin_beta=FE(7.2=100)
A:
NA
C2:
PF0036213=Integrin_beta=FE(6.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CCTTCTATTGCTCACCTTGTCCA
R:
ATTGTATGCATCAATGATCAACTGA
Band lengths:
180-473
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