Special

DreEX6097156 @ danRer10

Exon Skipping

Gene
Description
fibrillin 3 [Source:HGNC Symbol;Acc:HGNC:18794]
Coordinates
chr22:4109271-4112429:-
Coord C1 exon
chr22:4112345-4112429
Coord A exon
chr22:4112109-4112234
Coord C2 exon
chr22:4109271-4109399
Length
126 bp
Sequences
Splice sites
3' ss Seq
TAACGTGTTTCTGTCCACAGATG
3' ss Score
12.07
5' ss Seq
CAGGTACAC
5' ss Score
7.29
Exon sequences
Seq C1 exon
NNNNNNGAATTCAAGACTATCTGCCCTCGAGGACCCGGAATCGCCAATCGCGGAGACATTCTGACTGGGAGACCCTTCTACAAAG
Seq A exon
ATGTGAATGAGTGTAAGGTGTTTAGGGGGCTCTGCACTCACGGCACGTGTCGAAACACTATCGGCAGCTTCAAGTGTCGCTGTGATAGTGGTTTCGCCCTGACAATGGAGGAGAGGAACTGCACAG
Seq C2 exon
ATATCGACGAATGTACGATCTCTCCGGACCTGTGTGGTCATGGTGTGTGTGTGAACACACCAGGCAGCTTCGAGTGCGAGTGTTTCGACGGCTACGAGAGCGGCTTTATGATGATGAAAAACTGCATGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000098237-'7-6,'7-5,8-6=AN
Average complexity
A_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:
PF0068312=TB=PD(14.3=20.7),PF0764510=EGF_CA=PU(0.1=0.0)
A:
PF0764510=EGF_CA=WD(100=95.3),PF0764510=EGF_CA=PU(0.1=0.0)
C2:
PF0764510=EGF_CA=WD(100=95.5),PF0764510=EGF_CA=PU(0.1=0.0)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TTCAAGACTATCTGCCCTCGAGG
R:
TGCAGTTTTTCATCATCATAAAGCCG
Band lengths:
202-328
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]