Special

RnoEX0082345 @ rn6

Exon Skipping

Gene
Description
solute carrier family 35 member C2 [Source:RGD Symbol;Acc:1311250]
Coordinates
chr3:161802896-161805765:-
Coord C1 exon
chr3:161805597-161805765
Coord A exon
chr3:161805427-161805510
Coord C2 exon
chr3:161802896-161803071
Length
84 bp
Sequences
Splice sites
3' ss Seq
TGTCGTGTCCTGTCCTGCAGGTC
3' ss Score
12.41
5' ss Seq
AAGGTACAC
5' ss Score
7.56
Exon sequences
Seq C1 exon
CGTGCAGCGCTGGTCCTGGTGGTCCTGCTCATTGCTGGCGGCCTCTTCATGTTTACCTATAAGTCCACGCAGTTCAACGTGGAGGGCTTTGCCTTGGTGCTGGGGGCTTCGTTCATTGGCGGCATCCGCTGGACCCTTACACAAATGCTTCTTCAGAAAGCTGATCTCG
Seq A exon
GTCTCCAGAATCCCATTGACACCATGTTCCACCTGCAGCCACTCATGTTTCTGGGGCTCTTCCCTCTCTTTGCCGTATTCGAAG
Seq C2 exon
GTCTCCATTTGTCCACCTCTGAGAAGATCTTCCGCTTCCAGGACCCGGGCCTGCTCCTGTGGGTTCTGGGGAGCCTCCTCCTCGGAGGGATTCTGGCCTTTGGCTTGGGCTTCTCTGAGTTCCTCTTGGTCTCCAGAACCTCGAGCCTCACACTCTCCATTGCTGGCATTTTTAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000018649_MULTIEX1-6/6=5-C2
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:
PF0315111=TPT=PU(18.5=49.1)
A:
PF0315111=TPT=FE(18.5=100)
C2:
PF0315111=TPT=FE(38.4=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CCGCTGGACCCTTACACAAAT
R:
GGAACTCAGAGAAGCCCAAGC
Band lengths:
167-251
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]