Special

HsaEX6039653 @ hg38

Exon Skipping

Gene
ENSG00000132932 | ATP8A2
Description
ATPase phospholipid transporting 8A2 [Source:HGNC Symbol;Acc:HGNC:13533]
Coordinates
chr13:25563956-25571692:+
Coord C1 exon
chr13:25563956-25564031
Coord A exon
chr13:25570767-25570872
Coord C2 exon
chr13:25571610-25571692
Length
106 bp
Sequences
Splice sites
3' ss Seq
ATCCCGCCTCACGTTTGCAGCCC
3' ss Score
8.16
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
Exon sequences
Seq C1 exon
TCGGATGCCTCCTCCCTGTAGTGATTCCTGTGACTTTGATGACCCCAGGCTGTTGAAGAACATTGAGGATCGCCAT
Seq A exon
CCCACAGCCCCTTGCATTCAGGAGTTCCTCACCCTTCTGGCCGTGTGCCACACGGTTGTTCCTGAGAAGGATGGAGATAACATCATCTACCAGGCCTCTTCCCCAG
Seq C2 exon
ATGAAGCTGCTTTGGTGAAAGGAGCTAAAAAGCTGGGCTTTGTCTTCACAGCCAGAACACCATTCTCAGTCATCATAGAAGCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000132932-'37-34,'37-32,40-34
Average complexity
C1
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.014 A=0.040 C2=0.000
Domain overlap (PFAM):

C1:
PF127102=HAD=FE(6.2=100)
A:
PF132461=Hydrolase_like2=PU(22.0=61.1)
C2:
PF132461=Hydrolase_like2=FE(27.0=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GATGCCTCCTCCCTGTAGTGA
R:
CGCTTCTATGATGACTGAGAATGGT
Band lengths:
156-262
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains