Special

HsaINT0108193 @ hg38

Intron Retention

Gene
Description
myosin X [Source:HGNC Symbol;Acc:HGNC:7593]
Coordinates
chr5:16780524-16780741:-
Coord C1 exon
chr5:16780728-16780741
Coord A exon
chr5:16780609-16780727
Coord C2 exon
chr5:16780524-16780608
Length
119 bp
Sequences
Splice sites
5' ss Seq
AAAGTAAGT
5' ss Score
9.72
3' ss Seq
AATCTGATTTATCTTCCCAGAAC
3' ss Score
7.4
Exon sequences
Seq C1 exon
ATTTATTAGAAAAA
Seq A exon
GTAAGTAAACGTGATTTAATCCACATTTTCTTCCATAATAACAATTTTCAGAAATTATTGGTTTGTGTGAATTAAGCACAGGACACATCTCTGAATATAAATCTGATTTATCTTCCCAG
Seq C2 exon
AACCGAGTAGTAAGGCAAAATCCCGGGGAAAGGAATTATCACATATTTTATGCACTGCTGGCAGGGCTGGAACATGAAGAAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000145555:ENST00000513610:7
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=0.000
Domain overlap (PFAM):

C1:
PF0006316=Myosin_head=FE(0.6=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(4.2=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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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