Special

HsaINT0107503 @ hg38

Intron Retention

Gene
Description
myosin heavy chain 11 [Source:HGNC Symbol;Acc:HGNC:7569]
Coordinates
chr16:15756341-15758000:-
Coord C1 exon
chr16:15757827-15758000
Coord A exon
chr16:15756515-15757826
Coord C2 exon
chr16:15756341-15756514
Length
1312 bp
Sequences
Splice sites
5' ss Seq
CCGGTGAGG
5' ss Score
9.35
3' ss Seq
GCCCTACTTGTCTCCCACAGAAC
3' ss Score
10.81
Exon sequences
Seq C1 exon
GTGAACTCCTTCGAGCAGCTGTGCATCAACTACACCAACGAGAAGCTGCAGCAGCTCTTCAACCACACCATGTTCATCCTGGAGCAGGAGGAGTACCAGCGCGAGGGCATCGAGTGGAACTTCATCGACTTTGGGCTGGACCTACAGCCCTGCATCGAGCTCATCGAGCGACCG
Seq A exon
GTGAGGGGCACGTGGGCGTGCGGGGCTCCGTCACACCTTGTACACGTGTGTGGCCTCTGTGGAGCCGACGTGGACCCCACACTCTCCCCATGCACATAGCATTCCCCCACCCAATCCATCACCCAGTCCTGAAAGGCTGTAAGCTGAATCCTTGTGAACTCTTACAATTTCCATTAACCCACATTTTCATATCAAAGGTATTTTCTTTAATTTCTGCCTTCCTTCCATCCTCTTTTTTCTTCCTTTTTTTCTTCCCTACCCTCTTTCCCTTCCCTTTCCTTCTCTGCCATTGCTTTTTTTTTTTTTTTTTTTTTTTTTATGACATGGTCTGACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTTGCCTCACTGCAACCTCCACCTCCCTGCCTCAAGTGATCCTCCCGCCTCAGCCTCCCAAGTGGCTGAGACTACAGGCGTGCACCACCACGCCCACCTAACTTTTGTATTTTCAGTAGAGACAGGGTTTCTACTAATTAGCCGGGCCTGGTGGTGCACGCCTGTGGTCCCAGCTATTTGGGAGGCTGAGGTGGGAGGATTGCTTGAGCCCTGGAGGCAGAGGTTGCTGTAAGCCGAGATTGCGCCACTGCATTCCAGCCTGGATAACAGAGTGAGACCCTGTCTCCAAAAAAAACTTTTCTAACAGGAACCCTAGGTGAATTCAAGTCAAGCAACAAATTCATTTGCAAGAATTATGAACTCGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATGGAGACCATCCTGGCTAACACGGTGAAACCCCGCCTCTACTAAAAATAGAAAAAATCAGCCGGGCGCCGTGGCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAAGCGGAGCTTGCAGTGAGTCGAGATCGCGCCACTGCACCGTCTGCCTGGGCGACAAGGCAAAACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAGAGTTATGAACTCTTCATGATGTTGCCTGCGTGTTGCCCACTAGGGGGCGGCAGCAAACATTATGTTCTGCCTTCCATCCCTGTTACTGGTCCATTGGGCACAGGGTAATTTGAAGGTAGATTTGGAAGCATGGGGGTCATAAACTCATCTTTATATGTGGGCAAATACAGTATCAGATCTCGGCGGATGCCCATGCGTTGTGTATAGTTGGCCAGCTCTTCATGGAATGCCTGAGGTTGGGTGTTCTCTCTGATTCAAGCCCTACTTGTCTCCCACAG
Seq C2 exon
AACAACCCTCCAGGTGTGCTGGCCCTGCTGGACGAGGAATGCTGGTTCCCCAAAGCCACGGACAAGTCTTTCGTGGAGAAGCTGTGCACGGAGCAGGGCAGCCACCCCAAGTTCCAGAAGCCCAAGCAGCTCAAGGACAAGACTGAGTTCTCCATCATCCATTATGCTGGGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000133392:ENST00000300036:13
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=0.052
Domain overlap (PFAM):

C1:
PF0006316=Myosin_head=FE(8.3=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(8.3=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:
GTGAACTCCTTCGAGCAGCTG
R:
CAGCATAATGGATGATGGAGAACTCA
Band lengths:
343-1655
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development