Special

DreEX6065228 @ danRer10

Exon Skipping

Gene
Description
multiple EGF-like-domains 11 [Source:ZFIN;Acc:ZDB-GENE-060503-252]
Coordinates
chr18:19218704-19239825:-
Coord C1 exon
chr18:19239651-19239825
Coord A exon
chr18:19224183-19224303
Coord C2 exon
chr18:19218704-19218867
Length
121 bp
Sequences
Splice sites
3' ss Seq
CGTCGCTCTGTTTTTTTCAGGGA
3' ss Score
11.57
5' ss Seq
AAGGTATGG
5' ss Score
9.26
Exon sequences
Seq C1 exon
CTGTCACCCCTTGACTGGTGAATGCTCATGTACGGCGGGATGGACGGGCCTATATTGTAACGAGACCTGTCCCCCGGGCTACTATGGAGAAGGATGTGGAGTGCCGTGCCAGTGTGCTAATGGAGCCGACTGCCACAGTCTCACCGGGGCCTGTATCTGTGCCCCGGGCTACACA
Seq A exon
GGAGATGACTGTTCCCAAACCTGCCCATCTGGACTATTTGGGACTAACTGCACTTCCATTTGCCACTGCCACAACCAGGCGTCCTGCTCACCAATCGATGGCTCCTGTATCTGTAAAGAAG
Seq C2 exon
GTTGGCAGGGTGTGGACTGTTCAATCCTGTGCTCCAGCGGGACCTGGGGTTTGGGCTGTAACCAGACTTGTTTGTGTGCCAATGGTGCGGCTTGTGACCCAATCGATGGCTCTTGTACCTGTTCCTCAGGATGGAGAGGGGAGCGCTGCCAGCAGCCGTGCCCC
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000062686-'8-10,'8-9,9-10=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=0.000
Domain overlap (PFAM):

C1:
PF0005319=Laminin_EGF=PD(79.2=64.4),PF126612=hEGF=PU(61.5=13.6)
A:
PF126612=hEGF=PD(23.1=7.3),PF0005319=Laminin_EGF=PU(43.5=48.8)
C2:
PF0005319=Laminin_EGF=PD(54.3=45.5)


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:
TGGTGAATGCTCATGTACGGC
R:
GCACCATTGGCACACAAACAA
Band lengths:
248-369
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]