HsaEX0027949 @ hg38
Exon Skipping
Gene
ENSG00000167110 | GOLGA2
Description
golgin A2 [Source:HGNC Symbol;Acc:HGNC:4425]
Coordinates
chr9:128265970-128267517:-
Coord C1 exon
chr9:128267458-128267517
Coord A exon
chr9:128266287-128266325
Coord C2 exon
chr9:128265970-128266020
Length
39 bp
Sequences
Splice sites
3' ss Seq
CCTTTGACTCTTCCCCACAGAAA
3' ss Score
11.04
5' ss Seq
GAAGTAACG
5' ss Score
2.34
Exon sequences
Seq C1 exon
TCTGCGACATGTGTCAATGGGGAGGGCCCTGCATCGTCTGCTAACCTGAAGGATCTGGAG
Seq A exon
AAACAACAGAACCAAGAAATTACGGATCAGTTGGAAGAA
Seq C2 exon
GAAAAGAAAGAATGCCACCAAAAGCAGGGAGCCCTAAGGGAGCAGTTACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000167110_MULTIEX3-2/2=C1-C2
Average complexity
C2
Mappability confidence:
100%=100=100%
Protein Impact
Alternative protein isoforms (No Ref)
No structure available
Features
Disorder rate (Iupred):
C1=0.650 A=0.808 C2=0.510
Domain overlap (PFAM):
C1:
PF0157614=Myosin_tail_1=PU(8.5=50.0)
A:
PF0157614=Myosin_tail_1=FE(10.3=100)
C2:
PF0157614=Myosin_tail_1=FE(13.7=100)

Main Skipping Isoform:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CGACATGTGTCAATGGGGAGG
R:
TAACTGCTCCCTTAGGGCTCC
Band lengths:
104-143
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