Special

RnoEX0083449 @ rn6

Exon Skipping

Gene
Description
slit guidance ligand 1 [Source:RGD Symbol;Acc:69307]
Coordinates
chr1:260899052-260900553:-
Coord C1 exon
chr1:260900482-260900553
Coord A exon
chr1:260899527-260899598
Coord C2 exon
chr1:260899052-260899123
Length
72 bp
Sequences
Splice sites
3' ss Seq
AGTGCCCCTCTGCTTTACAGACA
3' ss Score
7.63
5' ss Seq
TCTGTGAGT
5' ss Score
7
Exon sequences
Seq C1 exon
GGACCTGAGTGAGAATTCTCTCCAGGCTGTGCCCAGAAAGGCTTTCCGAGGAGCCACAGACCTCAAAAATCT
Seq A exon
ACAGCTGGACAAGAACCAGATCAGCTGCATCGAGGAAGGGGCCTTCCGTGCCCTACGGGGACTGGAGGTTCT
Seq C2 exon
GACCCTGAACAACAACAACATCACCACCATCCCTGTGTCCAGTTTCAACCATATGCCCAAGCTTCGGACCTT
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000026065-'8-5,'8-4,9-5
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

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

C1:
PF138551=LRR_8=PU(8.2=20.0)
A:
PF138551=LRR_8=FE(39.3=100)
C2:
PF138551=LRR_8=FE(39.3=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
GGACCTGAGTGAGAATTCTCTCC
R:
AGGTCCGAAGCTTGGGCATAT
Band lengths:
143-215
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]