Special

HsaINT1016874 @ hg38

Intron Retention

Gene
Description
integrin subunit beta 1 [Source:HGNC Symbol;Acc:HGNC:6153]
Coordinates
chr10:32910223-32911670:-
Coord C1 exon
chr10:32911448-32911670
Coord A exon
chr10:32910456-32911447
Coord C2 exon
chr10:32910223-32910455
Length
992 bp
Sequences
Splice sites
5' ss Seq
TAAGTAAGT
5' ss Score
8.07
3' ss Seq
ATTTGTGTTTTTTGTAACAGAGA
3' ss Score
8.6
Exon sequences
Seq C1 exon
GAAATGGTGTTTGCAAGTGTCGTGTGTGTGAGTGCAACCCCAACTACACTGGCAGTGCATGTGACTGTTCTTTGGATACTAGTACTTGTGAAGCCAGCAACGGACAGATCTGCAATGGCCGGGGCATCTGCGAGTGTGGTGTCTGTAAGTGTACAGATCCGAAGTTTCAAGGGCAAACGTGTGAGATGTGTCAGACCTGCCTTGGTGTCTGTGCTGAGCATAA
Seq A exon
GTAAGTATTTCCTAATTGCTTGAAATAGTTGATACTTCCTCTTGGCTCTCCTAAGCCTGTATTGTTTCTAGAACCAGAACAGTGCCAATATTAAAATATACTGTAAATAAAATGCCTGCCATGTGGAAGCCTACTCTTTAATTCTTAAAAGTTCTTTCTCAACAGCTAGTATATATTACATGGTATGAAGTGTGTCATGTGAGAGTTGTACTATTATTTTGATCTGAATGTGCTAGATAATTGAATTTACATGGTAACCTTTATTTTGGCAATTAAGATTTAATTTAATTTAATTTGTCATTACCAATTTCTTAATTACTGTCTTTTGACAAAACTAAGCCAAATTAAAGATTTTTCCTCTTGAAGGATTATTATACTAGTAACATATTATTTAAATTATTATGATTTTGGCCGAGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGAAGGCCGAGACAGGTGGATCACTTAAGGTCAGGAGTTTGAGACCAGTCTGGCCAATGTGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGATATGGTGGTGTGTGCCTGTAATCTCAACTACTTGGGAGGTTGAGGCTTGCTTGAACCCGAGAGGCAGAGGTTACAGTGAGCCAAGGTCACACCACTGCACTGCCTGGATGACAGAACAAGACTCCATCGCAAAAAAAAAATTATTATGATTTTATGTTACATATTTAATATGTGATAGGGCTAATTTATTTTACTATCTTTTATTTCTTAATAGGGTTTTAATTTGAACTGTAATAAATCTTTAATTTTATTATGGAAATTAGCATCTTTTTACATAATTTTTCTATCCACAAATGTAATGTTCCTCTTCATTTATTGAAATCTTCCTTCATAGCTGTTTGTTCAATTTGGTCACAAGAGTTTAGCATGGGAAATATGTTTAAGCAAATATTTACTGAAATAATAAAATGTAAATATCATAATTTGTGTTTTTTGTAACAG
Seq C2 exon
AGAATGTGTTCAGTGCAGAGCCTTCAATAAAGGAGAAAAGAAAGACACATGCACACAGGAATGTTCCTATTTTAACATTACCAAGGTAGAAAGTCGGGACAAATTACCCCAGCCGGTCCAACCTGATCCTGTGTCCCATTGTAAGGAGAAGGATGTTGACGACTGTTGGTTCTATTTTACGTATTCAGTGAATGGGAACAACGAGGTCATGGTTCATGTTGTGGAGAATCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000150093:ENST00000302278:13
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=0.025
Domain overlap (PFAM):

C1:
PF079748=EGF_2=PD(64.5=26.7),PF079748=EGF_2=WD(100=42.7),PF079657=Integrin_B_tail=PU(4.5=5.3)
A:
NA
C2:
PF079657=Integrin_B_tail=FE(87.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TTGCAAGTGTCGTGTGTGTGA
R:
GGGACACAGGATCAGGTTGGA
Band lengths:
350-1342
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains