Special

HsaEX6063768 @ hg19

Exon Skipping

Gene
ENSG00000197859 | ADAMTSL2
Description
ADAMTS-like 2 [Source:HGNC Symbol;Acc:14631]
Coordinates
chr9:136426320-136433608:+
Coord C1 exon
chr9:136426320-136426417
Coord A exon
chr9:136432058-136432184
Coord C2 exon
chr9:136433395-136433608
Length
127 bp
Sequences
Splice sites
3' ss Seq
CACCCCTGTCCCCAACCCAGGGG
3' ss Score
6.39
5' ss Seq
CAGGTACCT
5' ss Score
8.16
Exon sequences
Seq C1 exon
GACCAGGCCCAAGGCGCGCAAGCAAGGCGTGAGTCCCGCGGACATGTACCGGTGGAAGCTCTCGTCCCACGAGCCCTGCAGTGCCACCTGCACCACAG
Seq A exon
GGGTCATGTCTGCGTACGCCATGTGTGTCCGCTATGATGGCGTCGAGGTGGATGACAGCTACTGTGACGCCCTGACCCGTCCCGAGCCTGTCCACGAGTTCTGCGCTGGGAGGGAGTGCCAGCCCAG
Seq C2 exon
GTGGGAGACGAGCAGCTGGAGCGAGTGTTCGCGCACCTGCGGAGAGGGCTACCAGTTCCGCGTCGTGCGCTGCTGGAAGATGCTCTCGCCCGGCTTCGACAGCTCCGTGTACAGCGACCTGTGCGAGGCAGCCGAGGCCGTGCGGCCCGAGGAACGCAAGACCTGCCGGAACCCCGCCTGCGGGCCCCAGTGGGAGATGTCGGAGTGGTCCGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197859-'12-14,'12-13,13-14=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.235 A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NO
C2:
PF0009014=TSP_1=WD(100=83.3)


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:
TACCGGTGGAAGCTCTCGTC
R:
ACTCCGACATCTCCCACTGG
Band lengths:
258-385
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains