HsaINT0062554 @ hg19
Intron Retention
Gene
ENSG00000142449 | FBN3
Description
fibrillin 3 [Source:HGNC Symbol;Acc:18794]
Coordinates
chr19:8145887-8146364:-
Coord C1 exon
chr19:8146242-8146364
Coord A exon
chr19:8146004-8146241
Coord C2 exon
chr19:8145887-8146003
Length
238 bp
Sequences
Splice sites
5' ss Seq
AAGGTGATG
5' ss Score
5.22
3' ss Seq
CTGGACCATCCGTGCTGCAGACC
3' ss Score
5.75
Exon sequences
Seq C1 exon
ATATGGATGAGTGCAGCCAGGTCCCCAAGCCATGTACCTTCCTCTGCAAAAACACGAAGGGCAGTTTCCTGTGCAGCTGTCCCCGAGGCTACCTGCTGGAGGAGGATGGCAGGACCTGCAAAG
Seq A exon
GTGATGTCCTTTCAACTCTCCCCCACTCCCACCACTGCATGCAGTCTAGGGCCCCAAAGGGATGCCCAAGACATGTCCCCTGCAATCTCACCCCCTCCCATCTGCATGGAGTCAAGCACCATCTCCGAGGTCTTTCTCTTGTCACCCCTCTGCCTGGAGGTGGCAAGGGCAGCCCCTGGGAAGCCCCTAATCCCCCACTGGGCCCTGCCCTGAGCCTGCTGGACCATCCGTGCTGCAG
Seq C2 exon
ACCTGGACGAATGCACCTCCCGGCAGCACAACTGTCAGTTCCTCTGTGTCAACACTGTGGGCGCCTTCACCTGCCGCTGTCCGCCCGGCTTCACCCAGCACCACCAGGCCTGCTTCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000142449-FBN3:NM_032447:57
Average complexity
IR-S
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=95.0),PF0764510=EGF_CA=PU(0.1=0.0)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GATGAGTGCAGCCAGGTCC
R:
GAAGCAGGCCTGGTGGTG
Band lengths:
234-472
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains
- Pre-implantation embryo development
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)