Special

HsaEX6077253 @ hg19

Exon Skipping

Gene
ENSG00000101251 | SEL1L2
Description
sel-1 suppressor of lin-12-like 2 (C. elegans) [Source:HGNC Symbol;Acc:15897]
Coordinates
chr20:13830837-13845887:-
Coord C1 exon
chr20:13845813-13845887
Coord A exon
chr20:13839908-13840080
Coord C2 exon
chr20:13830837-13830965
Length
173 bp
Sequences
Splice sites
3' ss Seq
TTCTCTAATATTTCTATCAGGCA
3' ss Score
6.45
5' ss Seq
AAGGTAATT
5' ss Score
8.83
Exon sequences
Seq C1 exon
AAAAGGCTAACATTCTTGAAAAAGAGAAGATGTATCCAATGGCGCTTCTCCTATGGAATCGAGCTGCCATTCAAG
Seq A exon
GCAATGCATTTGCTAGAGTAAAAATTGGAGATTACCATTACTATGGCTATGGGACTAAGAAAGACTATCAAACAGCAGCCACACACTACAGCATTGCAGCCAACAAATACCACAACGCGCAAGCCATGTTCAATCTGGCTTATATGTATGAACACGGCTTAGGCATCACAAAG
Seq C2 exon
GACATTCACTTGGCCAGAAGATTGTACGACATGGCTGCTCAAACGAGTCCAGATGCCCACATACCTGTGCTCTTTGCCGTCATGAAACTGGAAACTACGCATTTGCTCCGGGATATCCTGTTTTTTAAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000101251-'23-29,'23-27,24-29=AN
Average complexity
A_C1
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

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

C1:
NO
A:
PF082387=Sel1=WD(100=62.1),PF082387=Sel1=PU(52.9=31.0)
C2:
PF082387=Sel1=PD(41.2=32.6)


Main Inclusion Isoform:


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AAGGCTAACATTCTTGAAAAAGAGA
R:
ACAGGATATCCCGGAGCAAATG
Band lengths:
194-367
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains