Special

DreINT0010638 @ danRer10

Intron Retention

Gene
Description
fibrillin 3 [Source:HGNC Symbol;Acc:HGNC:18794]
Coordinates
chr22:4092779-4093118:-
Coord C1 exon
chr22:4092993-4093118
Coord A exon
chr22:4092896-4092992
Coord C2 exon
chr22:4092779-4092895
Length
97 bp
Sequences
Splice sites
5' ss Seq
TGGGTGAGT
5' ss Score
8.73
3' ss Seq
AATGTCTGTGTTTCTGGCAGATA
3' ss Score
10.29
Exon sequences
Seq C1 exon
ATCGTAACGAGTGTCAGGAGATCCCGAACGTCTGCAGTCACGGCGAGTGCATCGACACACAGGGCAGTTTCCGATGTCTGTGCCACAACGGCTTCAAAACTACGCCGGACCAGACCATGTGTATGG
Seq A exon
GTGAGTGTCCAACGCTACTGGAAGTGCATCTGCTTTTGTGGCTGTTTGAATGTGTAACAAGCTGTGGTAACTAACTAAATGTCTGTGTTTCTGGCAG
Seq C2 exon
ATATCGATGAATGTGACAGACAGCCGTGTGGAAACGGGACGTGTAAGAACACAGTGGGCTCCTACAACTGTCTGTGCTTCCCCGGGTTCGAGCTCACACATAATAATGACTGCATGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000098237:ENSDART00000167748:24
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF062476=Plasmod_Pvs28=FE(27.1=100),PF0764510=EGF_CA=WD(100=95.3),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF062476=Plasmod_Pvs28=PD(22.6=87.5),PF0764510=EGF_CA=WD(100=95.0),PF0764510=EGF_CA=PU(0.1=0.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCAGGAGATCCCGAACGTCTG
R:
AGTTGTAGGAGCCCACTGTGT
Band lengths:
182-279
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]