Special

HsaINT0082964 @ hg38

Intron Retention

Gene
Description
integrin subunit beta 8 [Source:HGNC Symbol;Acc:HGNC:6163]
Coordinates
chr7:20398860-20402126:+
Coord C1 exon
chr7:20398860-20398994
Coord A exon
chr7:20398995-20401720
Coord C2 exon
chr7:20401721-20402126
Length
2726 bp
Sequences
Splice sites
5' ss Seq
GAAGTATGT
5' ss Score
6.97
3' ss Seq
CTTTTTCCTCCTAAATTTAGGTT
3' ss Score
10.71
Exon sequences
Seq C1 exon
AAGCTCATTTCAGAAGTGAAAGTTCAGGTGGAAAACCAGGTACAAGGCATCTATTTTAACATTACCGCCATCTGTCCAGATGGGTCCAGAAAGCCAGGCATGGAAGGATGCAGAAACGTGACGAGCAATGATGAA
Seq A exon
GTATGTGGGTGTGCATTTTTCCCTTTTAAAATAAACTAAGTTGTTTGGCGTACTTTCTTACAGAAAAAGCAAACCATTCTGAAAAATTTTACTTACTACTGACTCTAAGAATCTTATTTATACTTCAAGGAAACTTTCATTGTCTCTCCTCAAAGTTCCTACTTGTTTTAGCTCAGCTGATTGTTCTCTCCAACTCTCAGGTTTTAATATGTATATGTGTGTGCGTGTGTGTGTAATATGAAACAATCATGTATCAATAGTAACTTTAAACTTAGGCGTCATGACCGGTATAAATTAGGAAATCACATATTCTCAAATAAGTAGTGTCTGTACTTATAATAATGATAATGCCTTTTTGATTTCATATTCACAAACTCTCAAAGTAAATGTAAAATTGAAAGTCACATATCACAGAAAAGAATGGGAATGATAGAACAGTTGATAAAGGCTAAGAATTTCAAAATCTTTCACTTTGTGATTGCCCCAGTACACTCATAATTATCTAAATTATCTAGAAGGAGGTAGGGAAATTTATTAAGAACAATACAAAATGGGAAGAGTCATCATTTACCAAAAAAAAAAAAATGGGATGTAAAGGAGAGAGATCCAGATTGTAACAGTATCAGGAAACAGCACCAGAGGAGATAGAGATTCTCCAAGGATTGGCACAACGGAGAGAGTAACACAAAGAAACATACTCTTTAAGGGAGTCTTTGCTGGGTGAAGTGATTTTGATTGAGTCATTTACGTCATGAGGCATTGTCTCATGTTTAAATGAATGACTTGGACTAGTAGATTTCCAACCCCTTTTAATCTAAAGTGCAATGATGATTAATTATGTAATGTCATGCTATAGAAAAAAAGAAAAAGTTATTGAAAGTGATAGAAGATTCTAAAAATGAATAAAAGAGACTCTTCTCTTTAGTTAGAATATGTTTTTCTATCTTAGGAATTTTAGAGCTGTGTATTTTAAATTAATTATTGCAAGTTTCTAATTCTGTGGTTTCTTCTATGATCACTCCGTGGATTTTGTTCAAAGGACATCATATACCAGTTTGCAAAATGCACTTTGGCTTTTCATTAAAACTACAGAGAAAACTTTTTACTAGCAAATATAGCACTAAGTTACTTTATGAAAAAACGCTTACTGTCTTAGAAATAGTTATTTCCTTCAAAATGTCATTTTGGAAGAATGGTTTTTCTTAGCTTTTACATTGTTTTTTTTCTTTTCATTTGCTTACATGCCATCTTTCCTTCATTTTCAATTGAGTAGTATAAATAGTTTAACTCTCAGGAATAGTCATATGACCTCTTAATTATAGAAACCCCAGAGTATGATCTACTGTTAGAGATGGCAGTGGCCACATTAACTTATGTATCTGTTAAGCTTCAGCATTCTCAAAGACAAAAGCATTTTAAGCATAACACCAACTGTATTGATTTTAATATTATGGAACAAATTCTAATGTTTCATGTATATATAAGCCAAATTTAGATACTTTATATTATTATATCGTAGATATATATTCCAACCAAAAAGCTCAGCGCAAATTAATTTTAAATTGTAATGGATCTCAATCCAACGTGAAAGAAATATACCTTCTTATTTACCAAAGTACCTAAAGATGGTAAGGTGAGCCAACAAATATAAATAGACATATTAAATCAATTGTGTTGTGCAAAAAGAAGAAATAGAGAAAAAGAAAACATTTGACCAATTCCTGCCAGCACAGCTCCTTAGTTCTGGGCTATCTTCTTCCATGGAGACAAATAGATAACCTGTGTTGAGGTCTTAAGATTTGCAAATGAGAGTCCTAAACATTTTTCTTTCGAGTAACATCAGAGAAGGCCACAGGTTTTCCTCCACTGAAACCCTGTATAAACTAAAATTTAACTCCGAAACTTTACTTGGGCTCCTAGAAAATAGGAACAAAATTAAAACTGTTCATTTGAACATCTTATCTCAGGGTTTTGATTTTTATTTATTTATTTATTTTTGAGATAGAGTCTCGCTGTGTCACTCAAGCTGTAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTCTGTCTTCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCTCCCAAGTAGCTGAGACTACAGGTGCGCGCCACCATGCTCAGCTAATTTTTGAATTTTTAGTAGAGATAGGGTTTCACCATGTTGGCTAGGCTGATCTCGAACTCCTGACCTCAAGTGATCCAACCGCCTAAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACGCCAGGCCTCATCTCAGGGTTTTAAACCAGTAGAGCAGAAGCCCTTTACTTTGGTTTATGTGATCTATCTCTAGTGTCAAATATTCAATACCCCACATTTTAATGGCTGAGTTTAGAAAATGGCCTATTCTTTCTCATGTTTGCTAAGAAATTAATCATCAGTGATGGGGTAGATGCTTCAGATAGGCTTGCACTCAAGTCTATTTAATGGTGCAATATAGGGATTAGTAGTTATTATATTCTTTAACCCTCAAGTTCATTCATTGGAAAATAAATGACTTTAAAAAGAGATGTTGCATATATATGAAAGAGATTACATGTGTTTCTTTTACAAATATCGTTAATTTCTCTAAGATGGTTTCTTATCAATTCAGTTATTAACAGATATAATATTGGTAATAAAAATAATTAAGGTATATAAATATATTTCCTTTTTCCTCCTAAATTTAG
Seq C2 exon
GTTCTTTTCAATGTAACAGTTACAATGAAAAAATGTGATGTCACAGGAGGAAAAAACTATGCAATAATCAAACCTATTGGTTTTAATGAAACCGCTAAAATTCATATACACAGAAACTGCAGCTGTCAGTGTGAGGACAACAGAGGACCTAAAGGAAAGTGTGTAGATGAAACTTTTCTAGATTCCAAGTGTTTCCAGTGTGATGAGAATAAATGTCATTTTGATGAAGATCAGTTTTCTTCTGAGAGTTGCAAGTCACACAAGGATCAGCCTGTTTGCAGTGGTCGAGGAGTTTGTGTTTGTGGGAAATGTTCATGTCACAAAATTAAGCTTGGAAAAGTGTATGGAAAATACTGTGAAAAGGATGACTTTTCTTGTCCATATCACCATGGAAATCTGTGTGCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000105855:ENST00000222573:9
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.022 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0036213=Integrin_beta=FE(10.6=100)
A:
NA
C2:
PF0036213=Integrin_beta=PD(12.3=30.1),PF079748=EGF_2=WD(100=26.5),PF079748=EGF_2=PU(28.6=7.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
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
  • Pre-implantation embryo development