Special

HsaINT0107735 @ hg19

Intron Retention

Gene
Description
myosin, heavy chain 3, skeletal muscle, embryonic [Source:HGNC Symbol;Acc:7573]
Coordinates
chr17:10542361-10542791:-
Coord C1 exon
chr17:10542615-10542791
Coord A exon
chr17:10542507-10542614
Coord C2 exon
chr17:10542361-10542506
Length
108 bp
Sequences
Splice sites
5' ss Seq
GACGTAAGT
5' ss Score
10.93
3' ss Seq
GGAAATGGTGCCTTTTTCAGCTG
3' ss Score
5.93
Exon sequences
Seq C1 exon
GTTAAAAACCTTACTGAGGAACTCTCTGGGTTAGATGAAACAATTGCAAAGTTAACCAGAGAGAAGAAGGCCCTCCAAGAGGCGCACCAGCAGGCCTTGGATGACCTCCAAGCTGAAGAAGACAAAGTCAATTCTTTGAACAAAACCAAGAGCAAACTGGAACAGCAAGTGGAAGAC
Seq A exon
GTAAGTAAATAATGCTCATCGGGAGTCCCAGAACTCCAGGGTTGGAAGAGCCCTCAAGGGTCCTCTTGCAAAGCATTTGTTCCCAAAAGGAAATGGTGCCTTTTTCAG
Seq C2 exon
CTGGAAAGCTCCCTAGAACAAGAAAAGAAGCTCCGAGTAGACCTGGAAAGGAACAAAAGGAAATTGGAAGGAGACTTGAAGCTTGCTCAAGAGTCCATATTAGATCTGGAGAATGACAAGCAACAGCTGGACGAAAGGCTCAAGAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000109063-MYH3:NM_002470:23
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.729 A=NA C2=0.020
Domain overlap (PFAM):

C1:
PF0157614=Myosin_tail_1=FE(29.4=100),PF0157614=Myosin_tail_1=PU(46.3=52.5)
A:
NA
C2:
PF0157614=Myosin_tail_1=PD(1.0=4.1),PF0157614=Myosin_tail_1=PD(50.7=69.4),PF0157614=Myosin_tail_1=PU(1.6=28.6)


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:
AGAGAAGAAGGCCCTCCAAGA
R:
AGCCTTTCGTCCAGCTGTTG
Band lengths:
258-366
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