RnoINT0059644 @ rn6
Intron Retention
Gene
ENSRNOG00000043219 | Fbn2
Description
fibrillin 2 [Source:RGD Symbol;Acc:620910]
Coordinates
chr18:53094773-53095506:-
Coord C1 exon
chr18:53095384-53095506
Coord A exon
chr18:53094905-53095383
Coord C2 exon
chr18:53094773-53094904
Length
479 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGG
5' ss Score
10.51
3' ss Seq
TTTTAATGACTGTTTTCTAGATC
3' ss Score
7.71
Exon sequences
Seq C1 exon
ACATCAACGAGTGTGCCCAGAACCCGCTGCTCTGCGCTTTCCGCTGCATGAACACCTTTGGATCCTATGAATGCACATGCCCAGTTGGCTACGCCCTCAGGGAAGACCAAAAGATGTGTAAAG
Seq A exon
GTAAGGCCACGGTCGAAGGGAGAAGGGCAACTTGACTTGCCTCATTGGGATATAGCCTACTTTGGGCATAGACCTCTCCTGGACACCTTTCTCCCAGAGCATTACAGGAAAAAAAATCATGTGGCAGCTTTGCTATAGATTTCCTCTCCTACACAACAGGACACTTAAAAGTATGTGGATGAGATGGCTCGAGCATCCCATTGCTGTCACGTGCCCAGGCCCTTAGTAAAGCAAAAGTTACCTTTCCCTAAACTCATTGTAAGGACCAGTCTGGAAAGTGTTGCACATCTGGACTAGAGCCAGCTGTTCAGAAGACCGGGTGCCTTCGTCCTCTGCCACACCAGATGACAACGTGACAAGAGTCAGAAGAGCAGAAGTGTTACTGAAAAATTGCTAATGCCTATCTCGCTAAATAGAACGTTCTGTTCTTAACTGATGTGTTTCTTCCCTTTTGATGCATTTTAATGACTGTTTTCTAG
Seq C2 exon
ATCTGGATGAATGCGCTGAGGGGCTTCACGACTGTGAGTCCAGAGGCATGATGTGTAAGAATCTGATCGGCACCTTCATGTGCATCTGCCCCCCTGGCATGGCCCGCAGGCCAGACGGAGAAGGCTGCGTAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000043219:ENSRNOT00000066548:47
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=95.2),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=95.6),PF0764510=EGF_CA=PU(0.1=0.0)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CATCAACGAGTGTGCCCAGAA
R:
CTACGCAGCCTTCTCCGTCT
Band lengths:
254-733
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]