HsaEX0035275 @ hg19
Exon Skipping
Gene
ENSG00000130702 | LAMA5
Description
laminin, alpha 5 [Source:HGNC Symbol;Acc:6485]
Coordinates
chr20:60911790-60912783:-
Coord C1 exon
chr20:60912646-60912783
Coord A exon
chr20:60911960-60912042
Coord C2 exon
chr20:60911790-60911842
Length
83 bp
Sequences
Splice sites
3' ss Seq
GCGTGCATGTCCATGAGCAGGTG
3' ss Score
3.96
5' ss Seq
GAGGCACCT
5' ss Score
-0.12
Exon sequences
Seq C1 exon
CCTGCCACTGCTCTGCTGAAGGCTCCCTGCACGCAGCCTGTGACCCCCGGAGTGGGCAGTGCAGCTGCCGGCCCCGTGTGACGGGGCTGCGGTGTGACACATGTGTGCCCGGTGCCTACAACTTCCCCTACTGCGAAG
Seq A exon
GTGCTGTGTGGTGGGATGGCACGTCCGTTGCTGCGGAGGGAGCAGGGAGGTGCGTGTTTTCAGGCCGTCCATGTGGATGAGAG
Seq C2 exon
CTGGCTCTTGCCACCCTGCCGGTCTGGCCCCAGTGGATCCTGCCCTTCCTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000130702_MULTIEX2-3/3=2-C2
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=0.000 C2=0.000
Domain overlap (PFAM):
C1:
PF0005319=Laminin_EGF=PD(0.1=0.0),PF0005319=Laminin_EGF=PU(91.8=95.7)
A:
NO
C2:
PF0005319=Laminin_EGF=PD(6.1=16.7)
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Rat
(rn6)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CACTGCTCTGCTGAAGGCTC
R:
AGGAAGGGCAGGATCCACTG
Band lengths:
183-266
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- The Cancer Genome Atlas (TCGA)
- Genotype-Tissue Expression Project (GTEx)
- 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)