Special

DreINT0010647 @ danRer10

Intron Retention

Gene
Description
fibrillin 3 [Source:HGNC Symbol;Acc:HGNC:18794]
Coordinates
chr22:4084412-4085042:-
Coord C1 exon
chr22:4084923-4085042
Coord A exon
chr22:4084535-4084922
Coord C2 exon
chr22:4084412-4084534
Length
388 bp
Sequences
Splice sites
5' ss Seq
AAGGTATGG
5' ss Score
9.26
3' ss Seq
CTGCTGTATTTTGTGTGCAGACA
3' ss Score
7.9
Exon sequences
Seq C1 exon
ACACTGACGAATGCTCCATTGGAAACCCTTGCGGAAATGGCACATGCTCAAACGTTCCTGGAGGTTTCGAGTGCTCCTGTCAGGAGGGATTTGAACCCGGACCCATGATGACCTGTGAAG
Seq A exon
GTATGGCCAAGATATGAGCAGAAAAAAGTCACACATTTTTACAAATATGTAAAAGTTTTATTTCTTTTCCGTATAAATCCAAATATTCTTACAAAAAAATGTACTGAAAACTTTAAAAAGAGTAAAAGTTTATCTTGAGATCCAAAATTTTCTAAAAGGTTTGTGTATTTTCACACCAAATTGTAAGAATTTAAGCAAATAATGCCATACATTTTGACAAAAGGAGTCACAAAAACAGGCAATTTTGGCCTCAGATATTAAAAATGTCCCTGCAAATTTCTGAGGAGACTAAAAAATGTATTTATTAAAGCACATTTTAAAATATTTTACGACATAACCATACTTTGTTAATGTTTTTTTGTTGCAATCTGCTGTATTTTGTGTGCAG
Seq C2 exon
ACATCAACGAGTGTGCGGTGAATCCTCTTCTCTGCGCTTTCCGCTGCGTCAACACCTTCGGCTCATACGAGTGCATGTGTCCAACAGGATATGTGCTGCGTGACGACAACCGCATGTGCAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000098237:ENSDART00000167748:32
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=95.1),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=95.2),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:
CACTGACGAATGCTCCATTGGA
R:
CTGCACATGCGGTTGTCGTC
Band lengths:
240-628
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]