Special

HsaEX0002073 @ hg38

Exon Skipping

Gene
Description
acyl-CoA synthetase long-chain family member 3 [Source:HGNC Symbol;Acc:HGNC:3570]
Coordinates
chr2:222924456-222928936:+
Coord C1 exon
chr2:222924456-222924595
Coord A exon
chr2:222927017-222927189
Coord C2 exon
chr2:222928862-222928936
Length
173 bp
Sequences
Splice sites
3' ss Seq
TCTCTAATTTTTTTCTTTAGCTT
3' ss Score
9.16
5' ss Seq
AAGGTAGTG
5' ss Score
5.56
Exon sequences
Seq C1 exon
GAAATCATGGATCGGATCTACAAAAATGTCATGAATAAAGTCAGTGAAATGAGTAGTTTTCAACGTAATCTGTTTATTCTGGCCTATAATTACAAAATGGAACAGATTTCAAAAGGACGTAATACTCCACTGTGCGACAG
Seq A exon
CTTTGTTTTCCGGAAAGTTCGAAGCTTGCTAGGGGGAAATATTCGTCTCCTGTTGTGTGGTGGCGCTCCACTTTCTGCAACCACGCAGCGATTCATGAACATCTGTTTCTGCTGTCCTGTTGGTCAGGGATACGGGCTCACTGAATCTGCTGGGGCTGGAACAATTTCCGAAG
Seq C2 exon
TGTGGGACTACAATACTGGCAGAGTGGGAGCACCATTAGTTTGCTGTGAAATCAAATTAAAAAACTGGGAGGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000123983_MULTIEX2-1/2=C1-2
Average complexity
S*
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.004 A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
PF0050123=AMP-binding=PD(11.9=78.7)
A:
PF0050123=AMP-binding=FE(12.2=100)
C2:
PF0050123=AMP-binding=FE(5.3=100)


Main Inclusion Isoform:


Main Skipping Isoform:
ENST00000357430fB8601


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GAAATCATGGATCGGATCTACAAAA
R:
TTGATTTCACAGCAAACTAATGGT
Band lengths:
195-368
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