Special

RnoEX6005670 @ rn6

Exon Skipping

Gene
ENSRNOG00000058420 | AABR07006033.1
Description
NA
Coordinates
chr1:214749640-214750613:+
Coord C1 exon
chr1:214749640-214749890
Coord A exon
chr1:214749983-214750166
Coord C2 exon
chr1:214750412-214750613
Length
184 bp
Sequences
Splice sites
3' ss Seq
CTGCTGCTGCCTGTATCCAGATC
3' ss Score
8.39
5' ss Seq
GCGGTAAGC
5' ss Score
8.99
Exon sequences
Seq C1 exon
GTGTTTGCAGCGGCTGGGGTGACCCCCACTACATCACATTTGACGGCACCTACTACACTTTTCTGGACAATTGCACATACGTGCTGGTGCAGCAGATTGTGCCTGTGTTTGGAGACTTCCGTGTGCTCATTGACAACTACTACTGTGACCTGGGAGACAGTGTTTCCTGCCCACAGTCCATCATTGTCGAGTACCACCAGGACCGTGTGGTGCTGACCCGCAGGCCGGTTCACGGGGTCATGACCAACCAG
Seq A exon
ATCATCTTCAACAACAAGGTCGTGAGTCCTGGCTTCCAGCAGAATGGCATTATCATCTCCCGTGTGGGTATCAAGATGTATGTCACCATCCAAGAGATTGGTGTCCAGGTCATGTTTTCAGGCCTCATCTTCTCAGTTGAGGTGCCCTTCAACTTGTTTGCCAACAACACGGAGGGCCAATGCG
Seq C2 exon
GCACTTGTACCAATGACAAAAAGGATGAATGCCGCCTGCCTGGAGGTTCCATAGCCTCCTCTTGTTCTGAGATGTCCCTCCACTGGAAGGTGCCCAACCAGCCTTCCTGCCAAGGGCCTCCACCAACACCAACTTCAATGGTACCCAGGTCTACACCTACTCCGTGCTCACCATCGCCACTCTGTCAGCTCATCCTAAGCGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000058420-'11-10,'11-9,12-10=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.000 C2=0.147
Domain overlap (PFAM):

C1:
PF0009420=VWD=PU(50.6=96.4)
A:
PF0009420=VWD=FE(38.1=100)
C2:
PF0009420=VWD=PD(10.0=23.5),PF087426=C8=PU(17.6=19.1)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Human
(hg38)
No conservation detected
Mouse
(mm10)
No conservation detected
Chicken
(galGal4)
Chicken
(galGal3)
No conservation detected
Zebrafish
(danRer10)
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GTTTCCTGCCCACAGTCCATC
R:
AGCACGGAGTAGGTGTAGACC
Band lengths:
258-442
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]