HsaEX6063443 @ hg19
Exon Skipping
Gene
ENSG00000187239 | FNBP1
Description
formin binding protein 1 [Source:HGNC Symbol;Acc:17069]
Coordinates
chr9:132720770-132741653:-
Coord C1 exon
chr9:132741597-132741653
Coord A exon
chr9:132740744-132740891
Coord C2 exon
chr9:132720770-132720832
Length
148 bp
Sequences
Splice sites
3' ss Seq
GCGTGTGTTCTGTTCCATAGGTA
3' ss Score
11.23
5' ss Seq
TCAGTAAGC
5' ss Score
5.59
Exon sequences
Seq C1 exon
GAATCTTTCAAAGAAGTACCAACCTAAAAAGAACTCGAAGGAGGAAGAAGAATACAA
Seq A exon
GTATACGTCATGTAAAGCTTTCATTTCCAACCTGAACGAAATGAATGATTACGCAGGGCAGCATGAAGTTATCTCCGAGAACATGGCATCACAGATCATTGTGGACTTGGCACGCTATGTTCAGGAACTGAAACAGGAGAGGAAATCA
Seq C2 exon
AACTTTCACGATGGCCGTAAAGCACAGCAGCACATCGAGACTTGCTGGAAGCAGCTTGAATCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000187239-'6-9,'6-8,7-9=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact
ORF disruption upon sequence exclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.190 A=0.091 C2=0.267
Domain overlap (PFAM):
C1:
PF0061118=FCH=FE(34.5=100),PF057016=WEMBL=PU(4.0=30.0)
A:
PF0061118=FCH=PD(29.8=56.0),PF057016=WEMBL=PU(29.6=80.0)
C2:
PF057016=WEMBL=FE(14.8=100)
Main Skipping Isoform:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GAATCTTTCAAAGAAGTACCAACCT
R:
TTCCAGCAAGTCTCGATGTGC
Band lengths:
107-255
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains
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)