Special

HsaINT0108824 @ hg38

Intron Retention

Gene
Description
myosin VB [Source:HGNC Symbol;Acc:HGNC:7603]
Coordinates
chr18:49835344-49836885:-
Coord C1 exon
chr18:49836711-49836885
Coord A exon
chr18:49835425-49836710
Coord C2 exon
chr18:49835344-49835424
Length
1286 bp
Sequences
Splice sites
5' ss Seq
CAGGTACAG
5' ss Score
8.68
3' ss Seq
TCCGTTTTTATCCCCAACAGATT
3' ss Score
9.64
Exon sequences
Seq C1 exon
GTACAATATAAGTCAGCTTGAGGAGTGGCTTCGGGGAAGAAACCTTCACCAGAGTGGAGCAGTTCAGACCATGGAACCTCTGATCCAAGCAGCCCAGCTCCTGCAATTAAAGAAGAAAACCCAGGAGGACGCAGAGGCTATCTGCTCCCTGTGTACCTCCCTCAGCACCCAGCAG
Seq A exon
GTACAGTCACTTTGCACCTCTGTCAACATGGTATTCCAAGGAAGCCCTGAGTCCATTCCAAGTCTGTTCTCGTTGGTGGTTATTTGTTAGTGTTGCACTCCCACCCTTTATATACCCCTAATGAGACAATTTTGAAGTGCAGCTGATGGGATATTCCTAGATGAACCAAAAACCATTTGGTCTGTGAAACAAGATGCCACAGATACTGTTTTCTAGTAACTCTCTATCCCTCTTACTCACTTAAAAAGATAAGGTAGCAAACTCACAAAACGTTAAGTTTAGGTAAAAACTTCTTTAAATATAATGAATTCTGGAATGTTTCTTACATAGAAATCCACAAATTTTCAGAAATTGGCAGCATCAGGTATTTGCTTTCTTTACAAATATAACTGTAAGAAAAACCTTTTCTTTAAAACTAATTGCAATATGGTCATATTTTCACTCACACTCATTTATATTGTTTTAAATGAAGTCATTAAGAACTTAGGGGCATTTAAGTGTTACTTTCCTTTTCCCTAAAAAATGTATAACCATGATTCAGTTGCCGACACATTGCCAGTCCCTGAAAGATAAATAACAAAATCCAAACTCAGTACAGAAAAACACATCTTAATATAGCAAAGTGAACACCTTTCCTTACCTCCTCTGCTTACTATTAAAATATTAAATATCTAACTCTTTAAAAAACTGCTTCCTTCTGTAAACATTTCCAGAAAGTCTTCAAACATTTTTCTTCTCTTTAAATACATTTCACTTAAAGTAAGTTTCCTTCTAGATGCAGCTGGCATTGCATTTGGGCAGTCTACTTCCACCAAACCAGTGGTAGGCAGACAAAAGAGTATCTCCTGTTCAAATACTCATTTGTAAACAATGTTGGGGGACAGGGGGTAGTTAGGTATTAAACAAGACCTTTCTCATCTAAGGTAAGATCTCCAGTACTCTTCAGAAGAAACCTTTAAATTACTAGTAGATATGAGGCTGAGGATTTCAGGCAACTGCATTCTAAACTCCTCATTGTGTATACCAATGAGCATAGTGGGGAGGGGCAGGTGGGTTTACAGGAGACATGAGTTCGGTGAGAGGGCTCAGATCCACCTGACAAAGCTGTGGGCTCTAGTTTCCTGGATGCAGGCTCCAAGTGTAAATGTCAGTCCAGCTCCATCTGTGTTGTGGGCCTTGTCTAAAGAGGATCATACTCTTGTACCAATGTCACATATTCTTTAAAGTTCAAAAGTTGTCTCATGTTCATTTAGCTCTGTGCTAAATTCCGTTTTTATCCCCAACAG
Seq C2 exon
ATTGTCAAAATTTTAAACCTTTATACTCCCCTGAATGAATTTGAAGAACGGGTAACAGTGGCCTTTATACGAACAATCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000167306:ENST00000285039:38
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:
PF0184314=DIL=FE(54.7=100)
A:
NA
C2:
PF0184314=DIL=PD(12.3=48.1)


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:
ACAATATAAGTCAGCTTGAGGAGTGG
R:
CTGGATTGTTCGTATAAAGGCCAC
Band lengths:
254-1540
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