Special

RnoEX0003585 @ rn6

Exon Skipping

Gene
ENSRNOG00000053339 | AABR07062512.1
Description
NA
Coordinates
chr4:180486127-180500933:-
Coord C1 exon
chr4:180500808-180500933
Coord A exon
chr4:180492978-180493153
Coord C2 exon
chr4:180486127-180486291
Length
176 bp
Sequences
Splice sites
3' ss Seq
AACCCATCCACATTTTCCAGGTA
3' ss Score
8.12
5' ss Seq
AATGTAAGT
5' ss Score
8.62
Exon sequences
Seq C1 exon
ACAACCCCGCCCTGTTCTGGTTCTCCAGGCACATCTCCCTGTGGGGGAGCATCTCCTTCAACCTGGCTGTGTTCATCAACCTGGCCGTGGCTCTCTTCTACCCATTCGGGGATGACGGCGATGAAG
Seq A exon
GTACGCTCTCCCCGCTGTTCTCAGCCCTCCTTTGGGTAGCAGTGGCGATCTGCACGTCTATGCTGTTCTTCTTCTCCAAGCCTGTGGGCATCCGGCCATTCCTTGTGTCTATCATGCTCAGATCAATATACACCATCGGTCTGGGGCCAACGCTAATACTTCTTGGTGCTGCCAAT
Seq C2 exon
CTATGCAATAAAATCGTGTTCCTGGTGAGTTTTGTGGGAAACCGAGGCACATTCACCCGAGGGTACCGAGCAGTCATTCTGGACATGGCCTTTCTTTACCACGTGGCCTATGTCTTGGTTTGCATGCTTGGCCTCTTCGTCCACGAGTTCTTCTACAGCTTCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000053339-'2-5,'2-4,3-5
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.024 A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
PF0052026=Ion_trans=PU(26.2=83.1)
C2:
PF0052026=Ion_trans=FE(23.8=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
TTCTCCAGGCACATCTCCCTG
R:
GAAGAGGCCAAGCATGCAAAC
Band lengths:
244-420
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]