Special

HsaEX0061891 @ hg19

Exon Skipping

Gene
Description
SCO-spondin homolog (Bos taurus) [Source:HGNC Symbol;Acc:21998]
Coordinates
chr7:149479270-149480422:+
Coord C1 exon
chr7:149479270-149479387
Coord A exon
chr7:149479935-149480110
Coord C2 exon
chr7:149480195-149480422
Length
176 bp
Sequences
Splice sites
3' ss Seq
CATCAGACCCCCTGTTCCAGGAG
3' ss Score
5.11
5' ss Seq
CAGGTGTGC
5' ss Score
6.46
Exon sequences
Seq C1 exon
GACTATGTGAAGGGACAGCTACTGATCCTACTGGAGCATGGGGCCTGCGACGCTGGGAGCTGCCTGCACGCCATCTCCGTCTCCCTGGAGGACACCCACATCCAGCTCAGGGACTCAG
Seq A exon
GAGCTGTGCTGGTCAATGGGCAGGATGTGGGCTTGCCCTGGATTGGCGCTGAGGGCCTCAGTGTGCGCCGAGCTTCCTCTGCCTTTCTGCTGCTGCGCTGGCCTGGGGCCCAGGTGCTCTGGGGACTGTCTGACCCTGTAGCCTACATCACCCTGGACCCCCGCCATGCCCACCAG
Seq C2 exon
GTGCAGGGTCTGTGTGGCACCTTCACCCAGAACCAGCAGGACGACTTCCTGACACCAGCCGGAGATGTGGAAACTAGCATTGCTGCCTTTGCTAGCAAGTTCCAGGTGGCCGGCAAGGGAAGATGCCCCTCTGAGGACAGTGCCCTGCTGTCTCCCTGCACCACCCACTCCCAGCGCCACGCCTTCGCAGAGGCGGCCTGTGCCATCCTGCACAGCTCTGTCTTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197558_CASSETTE1
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.140 A=0.000 C2=0.007
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:
ACATCCAGCTCAGGGACTCAG
R:
AAGACAGAGCTGTGCAGGATG
Band lengths:
245-421
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development