Special

HsaEX6057495 @ hg38

Exon Skipping

Gene
Description
myosin heavy chain 15 [Source:HGNC Symbol;Acc:HGNC:31073]
Coordinates
chr3:108470042-108476515:-
Coord C1 exon
chr3:108476397-108476515
Coord A exon
chr3:108470698-108470847
Coord C2 exon
chr3:108470042-108470212
Length
150 bp
Sequences
Splice sites
3' ss Seq
GTTTTCAATGTGATTTCTAGGTA
3' ss Score
7.99
5' ss Seq
GAGGTAAGT
5' ss Score
11.08
Exon sequences
Seq C1 exon
ATGCTGACAAAGCTGCTTTCCTCATGGGCATTAACTCCTCTGAGTTGGTAAAGTGCTTGATCCATCCTAGAATCAAAGTTGGTAACGAATATGTTACCAGAGGTCAAACTATAGAACAG
Seq A exon
GTAACCTGTGCTGTCGGTGCCCTGTCCAAGTCAATGTATGAAAGGATGTTTAAGTGGCTAGTGGCACGGATCAACAGGGCCCTGGATGCCAAGCTGTCAAGGCAGTTCTTCATTGGCATTCTTGACATCACTGGTTTTGAAATCCTTGAG
Seq C2 exon
TATAATAGCCTTGAGCAACTTTGCATTAATTTTACCAATGAAAAATTACAACAATTCTTCAATTGGCACATGTTTGTTCTGGAGCAAGAGGAATATAAGAAAGAAAGCATTGAATGGGTGTCTATTGGCTTTGGTCTGGATTTGCAAGCTTGCATAGATCTCATTGAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000144821-'16-17,'16-16,20-17=AN
Average complexity
A_C2
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

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

C1:
PF0006316=Myosin_head=FE(5.8=100)
A:
PF0006316=Myosin_head=FE(7.3=100)
C2:
PF0006316=Myosin_head=FE(8.3=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AAAGCTGCTTTCCTCATGGGC
R:
TGCAAATCCAGACCAAAGCCA
Band lengths:
257-407
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains