Special

HsaEX6074517 @ hg38

Exon Skipping

Gene
ENSG00000137872 | SEMA6D
Description
semaphorin 6D [Source:HGNC Symbol;Acc:HGNC:16770]
Coordinates
chr15:47759745-47761038:+
Coord C1 exon
chr15:47759745-47759907
Coord A exon
chr15:47760304-47760415
Coord C2 exon
chr15:47760978-47761038
Length
112 bp
Sequences
Splice sites
3' ss Seq
TAGCCCATTTTTACTTGCAGATT
3' ss Score
7.48
5' ss Seq
CAGGTAATT
5' ss Score
8.55
Exon sequences
Seq C1 exon
GTAGCTCAGTGGCATTTCTGAGCAGGGGCCACCCTGACTTCACCTTGGCCCACCATGAGGGTCTTCCTGCTTTGTGCCTACATACTGCTGCTGATGGTTTCCCAGTTGAGGGCAGTCAGCTTTCCTGAAGATGATGAACCCCTTAATACTGTCGACTATCACT
Seq A exon
ATTCAAGGCAATATCCGGTTTTTAGAGGACGCCCTTCAGGCAATGAATCGCAGCACAGGCTGGACTTTCAGCTGATGTTGAAAATTCGAGACACACTTTATATTGCTGGCAG
Seq C2 exon
GGATCAAGTTTATACAGTAAACTTAAATGAAATGCCCAAAACAGAAGTAATACCCAACAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137872-'35-40,'35-39,37-40
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.002 C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
PF0140314=Sema=PU(17.6=42.1)
C2:
PF0140314=Sema=FE(12.3=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCAGTGGCATTTCTGAGCAGG
R:
TTGTTGGGTATTACTTCTGTTTTGGG
Band lengths:
218-330
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains