HsaEX0026123 @ hg19
Exon Skipping
Gene
ENSG00000137942 | FNBP1L
Description
formin binding protein 1-like [Source:HGNC Symbol;Acc:20851]
Coordinates
chr1:93987639-93989880:+
Coord C1 exon
chr1:93987639-93987692
Coord A exon
chr1:93988901-93989048
Coord C2 exon
chr1:93989818-93989880
Length
148 bp
Sequences
Splice sites
3' ss Seq
TTTTGAAATGTTTTTGCCAGGTT
3' ss Score
6.6
5' ss Seq
ATGGTAATT
5' ss Score
6.49
Exon sequences
Seq C1 exon
AAATCTGGTTAAGAAGTACTGCCCCAAACGTTCATCCAAAGATGAAGAGCCACG
Seq A exon
GTTTACCTCGTGTGTAGCCTTTTTTAATATCCTTAATGAGTTAAATGACTATGCAGGACAGCGAGAAGTTGTAGCAGAAGAAATGGCGCACAGAGTGTATGGTGAATTAATGAGATATGCTCATGATCTGAAAACTGAAAGAAAAATG
Seq C2 exon
CATCTGCAAGAAGGACGAAAAGCTCAACAATATCTTGACATGTGCTGGAAACAGATGGATAAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137942-'2-5,'2-4,4-5
Average complexity
S
Mappability confidence:
88%=100=75%
Protein Impact
ORF disruption upon sequence exclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.075 A=0.056 C2=0.050
Domain overlap (PFAM):
C1:
PF0061118=FCH=FE(21.7=100),PF049318=DNA_pol_phi=FE(17.0=100),PF0765111=ANTH=FE(18.2=100)
A:
PF0061118=FCH=PD(30.1=56.0)
C2:
NO
Main Skipping Isoform:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AAATCTGGTTAAGAAGTACTGCCCC
R:
ATCCATCTGTTTCCAGCACATGT
Band lengths:
114-262
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)