Special

HsaINT0107526 @ hg38

Intron Retention

Gene
Description
myosin heavy chain 11 [Source:HGNC Symbol;Acc:HGNC:7569]
Coordinates
chr16:15719220-15719713:-
Coord C1 exon
chr16:15719585-15719713
Coord A exon
chr16:15719309-15719584
Coord C2 exon
chr16:15719220-15719308
Length
276 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAAG
5' ss Score
8.27
3' ss Seq
CCTTCCTCCCTCCCACCTAGGAC
3' ss Score
10.82
Exon sequences
Seq C1 exon
GCTCAGATGAAGGACTTTCAAAGAGAGCTGGAAGATGCCCGTGCCTCCAGAGATGAGATCTTTGCCACAGCCAAAGAGAATGAGAAGAAAGCCAAGAGCTTGGAAGCAGACCTCATGCAGCTACAAGAG
Seq A exon
GTAAAGCCTCGCCTTGCTAGGAGAGCCTCAGATGCGGGTGTCACGGTAGCACCCCTTGGCAGCTCCAGTCTGTGCATTCCCAGATTTCATTTCGTCCTCCTCTGGGGTCCACCTGTCTAGAAAGACACACGCTTCCCTCCTCTATGTATTCACGGGGCCTCCCCTGAGCTCAGAGGAAGAACATGTACTTTCAAGGGTGGCTGAGTTGTCAGGGTGGACTCTTGGTGGGGCTTGGCCTTTCCCTGGCAGACAACAGCCTTCCTCCCTCCCACCTAG
Seq C2 exon
GACCTCGCCGCCGCTGAGAGGGCTCGCAAACAAGCGGACCTCGAGAAGGAGGAACTGGCAGAGGAGCTGGCCAGTAGCCTGTCGGGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000133392:ENST00000300036:35
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.721 A=NA C2=1.000
Domain overlap (PFAM):

C1:
PF0157614=Myosin_tail_1=FE(4.9=100)
A:
NA
C2:
PF0157614=Myosin_tail_1=FE(3.4=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:
AGGACTTTCAAAGAGAGCTGGA
R:
GCTACTGGCCAGCTCCTCT
Band lengths:
197-473
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