Special

HsaEX6063750 @ hg19

Exon Skipping

Gene
ENSG00000160323 | ADAMTS13
Description
ADAM metallopeptidase with thrombospondin type 1 motif, 13 [Source:HGNC Symbol;Acc:1366]
Coordinates
chr9:136295059-136298649:+
Coord C1 exon
chr9:136295059-136295221
Coord A exon
chr9:136297709-136297813
Coord C2 exon
chr9:136298498-136298649
Length
105 bp
Sequences
Splice sites
3' ss Seq
CCACCTGTCCACCCTCCTAGGAT
3' ss Score
9.19
5' ss Seq
AAGGTCAGA
5' ss Score
6.8
Exon sequences
Seq C1 exon
CGCAGGACGGGCGCGCTGCGTGTGGGACCCGCCGCGGCCTCAACCCGGGTCCGCGGGGCACCCGCCGGATGCGCAGCCTGGCCTCTACTACAGCGCCAACGAGCAGTGCCGCGTGGCCTTCGGCCCCAAGGCTGTCGCCTGCACCTTCGCCAGGGAGCACCTG
Seq A exon
GATATGTGCCAGGCCCTCTCCTGCCACACAGACCCGCTGGACCAAAGCAGCTGCAGCCGCCTCCTCGTTCCTCTCCTGGATGGGACAGAATGTGGCGTGGAGAAG
Seq C2 exon
TGGTGCTCCAAGGGTCGCTGCCGCTCCCTGGTGGAGCTGACCCCCATAGCAGCAGTGCATGGGCGCTGGTCTAGCTGGGGTCCCCGAAGTCCTTGCTCCCGCTCCTGCGGAGGAGGTGTGGTCACCAGGAGGCGGCAGTGCAACAACCCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000160323-'10-13,'10-12,12-13=AN
Average complexity
A_C1
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.283 A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
PF0142114=Reprolysin=PD(5.3=20.0)
A:
PF135821=Reprolysin_3=PD(3.3=11.1)
C2:
PF0009014=TSP_1=PU(53.8=54.9)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CAGCCTGGCCTCTACTACAGC
R:
CTGGGGTTGTTGCACTGCC
Band lengths:
242-347
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains