Special

HsaEX0041173 @ hg19

Exon Skipping

Gene
Description
myosin IIIA [Source:HGNC Symbol;Acc:7601]
Coordinates
chr10:26482134-26501456:+
Coord C1 exon
chr10:26482134-26482240
Coord A exon
chr10:26490194-26490234
Coord C2 exon
chr10:26500772-26501456
Length
41 bp
Sequences
Splice sites
3' ss Seq
TGAATTCTTCTTTCCTTTAGAAG
3' ss Score
7.86
5' ss Seq
CAGGTAATT
5' ss Score
8.55
Exon sequences
Seq C1 exon
GTGTCTGTAAAGGAGAGGAGCCAAAAATATTGAGACCCCCAAGACGACCCCGGAAACCCAAAACATTAAATAACCCTGAAGACTCCACATACTATTATCTACTTCAT
Seq A exon
AAGTCAATCCAAGAAGAAAAACGAAGACCAAGGAAAGACAG
Seq C2 exon
GTGCTGGGCGGCGGAGAGCCCCGAGAAGGAGGAGGAGAGAGAGCCAGCAGCCAACCCCTACGACTTCAGGAGGCTCCTGCGCAAAACCTCCCAGCGCCGGCGCCTCGTCCAGCAGTCCTAACCGTTCAACGAGGCAGTCACCGCCGTCGGAAGGCGCTGGAGCCTGCGGGGCAGCAGGGGCCAAGCAGGCACTCTGGGGCTGGCACCAGCAGGCACTGAAGCTGCGGCCCTGATCTCCGCAGAGGCTGCCTGCTGCGCTCGGCCCTCAAGTGCCCGGGCCGGCCTTCGTGCTCCGAAACAAGAGACCTGGGAGCCCTCGGGAAACCTCCCCCGACGCTCTCTCTCGGAACTCCCGCACCCTCCTTTCTCACCAGCCCGCCAGTTGTGGCAACCCTGTCCTTGTTCCCCTAATCTATCACTTTGTTCTTTTTTTTTGTGACTCCTGTGGACTCCACTGCGCCTGGGATCTCGCCAACCCCTCTCTCATTTGGGGTGACTGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000095777_MULTIEX1-16/17=15-C2
Average complexity
C3
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.556 A=0.643 C2=0.725
Domain overlap (PFAM):

C1:
NO
A:
NO
C2:
PF0006316=Myosin_head=PD(0.4=1.4)


Main Inclusion Isoform:


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GACCCCGGAAACCCAAAACAT
R:
CCTCCTGAAGTCGTAGGGGTT
Band lengths:
135-176
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • The Cancer Genome Atlas (TCGA)
  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development