Special

HsaEX0057077 @ hg38

Exon Skipping

Gene
ENSG00000001617 | SEMA3F
Description
semaphorin 3F [Source:HGNC Symbol;Acc:HGNC:10728]
Coordinates
chr3:50182284-50183018:+
Coord C1 exon
chr3:50182284-50182403
Coord A exon
chr3:50182644-50182783
Coord C2 exon
chr3:50182904-50183018
Length
140 bp
Sequences
Splice sites
3' ss Seq
CTGACCCCTGCCACCTGCAGACC
3' ss Score
9.5
5' ss Seq
CTGGTATGC
5' ss Score
6.73
Exon sequences
Seq C1 exon
ATGAGGAGCTCTATGCTGGTGTGTACATCGATTTTATGGGCACTGATGCAGCCATCTTCCGCACACTTGGAAAGCAGACAGCCATGCGCACGGATCAGTACAACTCCCGGTGGCTGAACG
Seq A exon
ACCCGTCGTTCATCCATGCTGAGCTCATTCCTGACAGTGCGGAGCGCAATGATGATAAGCTTTACTTCTTCTTCCGTGAGCGGTCGGCAGAGGCGCCGCAGAGCCCCGCGGTGTACGCCCGCATCGGGCGCATTTGCCTG
Seq C2 exon
AACGATGACGGTGGTCACTGTTGCCTGGTCAACAAGTGGAGCACATTCCTGAAGGCGCGGCTCGTCTGCTCTGTCCCGGGCGAGGATGGCATTGAGACTCACTTTGATGAGCTCC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000001617_MULTIEX1-1/2=C1-2
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=0.008 C2=0.000
Domain overlap (PFAM):

C1:
PF0140314=Sema=FE(19.2=100)
A:
PF0140314=Sema=FE(10.7=100)
C2:
PF0140314=Sema=FE(11.8=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:
GCTCTATGCTGGTGTGTACATCG
R:
GGAGCTCATCAAAGTGAGTCTCA
Band lengths:
228-368
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