Special

HsaEX1002694 @ hg38

Exon Skipping

Gene
ENSG00000160323 | ADAMTS13
Description
ADAM metallopeptidase with thrombospondin type 1 motif 13 [Source:HGNC Symbol;Acc:HGNC:1366]
Coordinates
chr9:133426199-133432692:+
Coord C1 exon
chr9:133426199-133426345
Coord A exon
chr9:133429944-133430101
Coord C2 exon
chr9:133432588-133432692
Length
158 bp
Sequences
Splice sites
3' ss Seq
CGGGCCTTGTCGCAGCGCAGGAC
3' ss Score
1.41
5' ss Seq
CTGGTGAGT
5' ss Score
10.1
Exon sequences
Seq C1 exon
GTTTGACCTGGAGTTGCCTGATGGTAACCGGCAGGTGCGGGGCGTCACCCAGCTGGGCGGTGCCTGCTCCCCAACCTGGAGCTGCCTCATTACCGAGGACACTGGCTTCGACCTGGGAGTCACCATTGCCCATGAGATTGGGCACAG
Seq A exon
GACGGGCGCGCTGCGTGTGGGACCCGCCGCGGCCTCAACCCGGGTCCGCGGGGCACCCGCCGGATGCGCAGCCTGGCCTCTACTACAGCGCCAACGAGCAGTGCCGCGTGGCCTTCGGCCCCAAGGCTGTCGCCTGCACCTTCGCCAGGGAGCACCTG
Seq C2 exon
GATATGTGCCAGGCCCTCTCCTGCCACACAGACCCGCTGGACCAAAGCAGCTGCAGCCGCCTCCTCGTTCCTCTCCTGGATGGGACAGAATGTGGCGTGGAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000160323_MULTIEX2-2/22=C1-3
Average complexity
C2*
Mappability confidence:
96%=100=96%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.040 A=0.254 C2=0.121
Domain overlap (PFAM):

C1:
PF135821=Reprolysin_3=FE(40.5=100)
A:
PF0142114=Reprolysin=PD(3.5=29.2)
C2:
PF135821=Reprolysin_3=PD(3.3=11.1)


Main Inclusion Isoform:
ENST00000474918fB8705


Main Skipping Isoform:


Other Skipping Isoforms:
NA
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTTTGACCTGGAGTTGCCTGA
R:
GCCACATTCTGTCCCATCCAG
Band lengths:
243-401
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains