Special

RnoINT0059632 @ rn6

Intron Retention

Gene
Description
fibrillin 2 [Source:RGD Symbol;Acc:620910]
Coordinates
chr18:53108194-53108617:-
Coord C1 exon
chr18:53108492-53108617
Coord A exon
chr18:53108320-53108491
Coord C2 exon
chr18:53108194-53108319
Length
172 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAAC
5' ss Score
8.14
3' ss Seq
TGGACCTGTGGTTCTTGCAGACA
3' ss Score
8.05
Exon sequences
Seq C1 exon
ACATTGACGAGTGTAAAGAGATTCCGGGCATCTGTGCAAACGGTGTGTGCATTAACCAGATCGGCAGTTTCCGCTGTGAATGCCCGACAGGCTTCAGTTACAACGACCTGCTCTTGGTCTGTGAAG
Seq A exon
GTAAACTGAGGAATTTATGTCCATCCTCCAAAGACTTTGCTATTTATAAGTGGCTTTTAGGTGGGCTTCCGGCTTTGGGCTACCTCCTCTGTCGAGTTTAAGAGCTGAGGACATGAATGTGACCCCAAAGCCATAGTGAGTGGCTGTTTACCTGGACCTGTGGTTCTTGCAG
Seq C2 exon
ACATCGATGAGTGCAGCAATGGTGACAACCTGTGCCAACGCAACGCGGACTGCATCAACAGCCCAGGCAGCTACCGCTGCGAGTGTGCGGCGGGCTTCAAGCTCTCCCCCAACGGGGCCTGTGTAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000043219:ENSRNOT00000066548:36
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:
PF0764510=EGF_CA=WD(100=95.3),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=95.3),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:
CGAGTGTAAAGAGATTCCGGGC
R:
CTACACAGGCCCCGTTGG
Band lengths:
245-417
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]