Special

HsaEX6011212 @ hg38

Exon Skipping

Gene
Description
SCO-spondin [Source:HGNC Symbol;Acc:HGNC:21998]
Coordinates
chr7:149790283-149791706:+
Coord C1 exon
chr7:149790283-149790620
Coord A exon
chr7:149791302-149791393
Coord C2 exon
chr7:149791475-149791706
Length
92 bp
Sequences
Splice sites
3' ss Seq
TTTCTCCTCTTCTTTCCCAGGGG
3' ss Score
11.81
5' ss Seq
CTGGTGAGG
5' ss Score
8.3
Exon sequences
Seq C1 exon
CGCCACCCTGCGGCCCCTTCGAGTTTCGGTGCGGCAGCGGCGAGTGCACCCCGCGGGGCTGGCGCTGCGACCAGGAGGAAGACTGCGCCGACGGCAGCGACGAGCGCGGCTGCGGAGGGCCCTGCGCGCCGCACCACGCGCCCTGCGCCCGCGGCCCTCACTGCGTGTCCCCCGAGCAGCTGTGCGACGGCGTGCGGCAGTGTCCCGACGGCTCGGACGAGGGCCCCGACGCCTGCGTTGAGGCTCCCGCGCCCCCGGCCATGCGCGGCCCCCCTGGCCAAGCCGGCGGGCCCACCTCTTCCCGAGCGCCATCCCCACCTTCGCCTCCTGAGGCACAG
Seq A exon
GGGGGCTGCCAGCCCTGGGAGGCCCCAACAGGACAGGGCTTCCCTGCCCAGAATACACCTGCCCCAATGGCACCTGCATAGGCTTCCAGCTG
Seq C2 exon
GTGTGTGATGGGCAGCCTGACTGTGGAAGGCCAGGGCAGGTGGGCCCCTCCCCAGAAGAGCAGGGTTGTGGGGCCTGGGGCCCCTGGAGCCCATGGGGGCCCTGCAGCCGGACGTGTGGGCCCTGGGGCCAGGGCCGGAGCCGCCGCTGCTCCCCACTCGGCCTCCTGGTGCTACAGAACTGCCCAGGGCCTGAGCACCAGTCTCAGGCCTGCTTCACGGCAGCCTGCCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197558_MULTIEX4-2/2=C1-C2
Average complexity
C2
Mappability confidence:
100%=100=100%
Protein Impact

NonCoding

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

C1:
NA
A:
NA
C2:
NA


Main Inclusion Isoform:
NA


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CAGTGTCCCGACGGCTCG
R:
CCTGGCCTTCCACAGTCAGG
Band lengths:
176-268
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains