Special

HsaINT0107497 @ hg19

Intron Retention

Gene
Description
myosin, heavy chain 10, non-muscle [Source:HGNC Symbol;Acc:7568]
Coordinates
chr17:8451631-8452105:-
Coord C1 exon
chr17:8451962-8452105
Coord A exon
chr17:8451727-8451961
Coord C2 exon
chr17:8451631-8451726
Length
235 bp
Sequences
Splice sites
5' ss Seq
TGTGTATGT
5' ss Score
3.3
3' ss Seq
TTCTTTTTATCAATATGAAGCAA
3' ss Score
3.16
Exon sequences
Seq C1 exon
CTGATTTGCTTCTTGAAGGATTTAATAACTACAGGTTTCTCTCCAATGGCTATATTCCTATTCCGGGACAGCAAGACAAAGATAATTTCCAGGAGACCATGGAAGCAATGCACATAATGGGCTTCTCCCATGAAGAGATTCTGT
Seq A exon
GTATGTGTGATTTCTCTAAGATTCTGGTACTCACTTTCCTAAGACTTATACATCTGGGGTAAATCACCTAAACTAGAAAATGACTGGGAAACTAATGAATTGTATGAAATCCTGAAAAGACATGTCTTACTGAAAAGTTTTGTATAGCTAATTTTTAGCACAAAATAAATGAGAATATGTCTCCGCTACATTTTGAGGCAATATTAATTTTTTTTTTCTTTTTATCAATATGAAG
Seq C2 exon
CAATGCTTAAAGTAGTATCTTCAGTGCTACAGTTTGGAAATATTTCTTTCAAAAAGGAGAGAAATACTGATCAAGCTTCCATGCCAGAAAATACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000133026-MYH10:NM_005964:9
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.020 A=NA C2=0.182
Domain overlap (PFAM):

C1:
PF0006316=Myosin_head=FE(7.0=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(4.7=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:
ACTACAGGTTTCTCTCCAATGGC
R:
CTGTATTTTCTGGCATGGAAGCT
Band lengths:
213-448
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