Special

HsaINT0107721 @ hg19

Intron Retention

Gene
Description
myosin, heavy chain 3, skeletal muscle, embryonic [Source:HGNC Symbol;Acc:7573]
Coordinates
chr17:10549024-10549349:-
Coord C1 exon
chr17:10549246-10549349
Coord A exon
chr17:10549163-10549245
Coord C2 exon
chr17:10549024-10549162
Length
83 bp
Sequences
Splice sites
5' ss Seq
GACGTAAGT
5' ss Score
10.93
3' ss Seq
TGCTGCCCTTTCCATGCCAGAGC
3' ss Score
8.24
Exon sequences
Seq C1 exon
AGCTGCTGCTTATTACGACCAACCCTTACGACTACCCGTTCATTAGCCAGGGGGAGATCCTGGTGGCCAGCATAGATGATGCAGAGGAGCTGCTGGCTACAGAC
Seq A exon
GTAAGTGGAACCAACAGAAGGGGTGGGTGTTCCTCCTCCATCACTGGGGCCAACTGACTGACGTGCTGCCCTTTCCATGCCAG
Seq C2 exon
AGCGCCATTGACATCCTGGGCTTCACCCCAGAAGAGAAATCTGGGCTCTACAAGCTGACGGGAGCCGTGATGCACTACGGGAACATGAAGTTCAAGCAGAAGCAGCGAGAGGAGCAGGCCGAGCCGGATGGCACAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000109063-MYH3:NM_002470:10
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.277
Domain overlap (PFAM):

C1:
PF0006316=Myosin_head=FE(5.0=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(6.8=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:
CATTAGCCAGGGGGAGATCCT
R:
CTCTCGCTGCTTCTGCTTGAA
Band lengths:
175-258
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